You are on page 1of 71

Tuầ n 1 tuan 4,5,6 bà i quizz

1. A unit of weight equal to 1/16th of a pound ounce (oz)

2. A unit of liquid volume equal to one thousandth of a liter and


equal to one cubic centimeter milliliter (ml)

3. a unit of mass equal to one millionth of a gram : microgram


(mcg)

4. If a patient c/o (complains of) something, he or she describes


symptoms that are painful or uncomfortable.

5. (Short of Breath) is a condition in which  a patient finds it more


difficult to breathe than usual : SOB

6. An intravenous injection is a method of administering


medicine into a vein using a syringe, often over a long period of
time : I.V

7. a unit of liquid volume equal to the amount of liquid which


comes from a dropper, or about 1/12th of a milliliter : drop (gtt)

8. An X-ray is a visual image of all or part of the body acquired


with special equipment using electromagnetic radiation to see
bones and other internal aspects of the body : XR

9. a unit of volume equal to a cube whose sides are equal to one


centimeter : cubic centimeter (cc)

10. If a function is WNL (Within Normal Limits), it is


operating in a normal range.

11. To give medicine to a patient : administer

12. If something is found o/e (on examination), it was


discovered during an exam.
13. (subcutaneous) A medicine that is injected into the fatty
layer under the skin with a syringe ; SQ

14. (sublingual) Medicine that is given beneath the tongue :


SL

15. the correct amount and frequency of medicine to give to


a person : dosage

16. (intramuscular injection) A medicine that is injected


into a muscle with a syringe : IM

17. A unit of mass equal to one thousandth of a gram :


milligram (mg)

18. (temperature) is a quantitative measurement of heat


within the body. It is can be used, in part, to gauge whether the
body is operating normally : T

19. Medicine is applied to a certain part of the surface of the


body : topical

20. a unit of mass which is equal to one-thousandth of a


kilogram : gram (g)

21. The path by which a medicine is taken into the body :


route of administration

22. 1/1000th the weight of the minor component of a


chemical solution dissolved in the major component :
milliequivalent (mEq)

23. (Diagnosis) is the positive identification of a patient's


disease or ailment : Dx

24. If a medicine is given P.R (per rectum), it is taken


through the rectum.

25. If medicine is given P.0 (by mouth), it is taken orally, or


through the mouth.
26. (Blood Pressure) is the force exerted by circulating
blood on the walls of blood vessels. Lt is a vital sign that medical
professionals use to determine whether body systems are
operating as they should : BP

27. A measure of volume equal to the amount a standard


tablespoon can hold or about three teaspoons: tablespoonful
(Tbsp)

28. (Heart Rate) is the frequency with which a person's


heart beats in a given amount of time. It is usually expressed in
beats per minute : HR

29. Drops of liquid administered to the eye : gtt

30. (hypertension) is having blood pressure that is higher


than normal : HTN

31. is the force exerted by circulating blood on the walls of


blood vessels. Lt is a vital sign that medical professionals use to
determine whether body systems are operating as they should

32. BP is the force exerted by circulating blood on the walls


of blood vessels. Lt is a vital sign that medical professionals use
to determine whether body systems are operating as they should

33. If a patient c/o something, he or she describes


symptoms that are painful or uncomfortable

34. Dx is the positive identification of a patient’s disease or


ailment.

35. HR is the frequency with which a person's heart beats in


a given amount of time. It is usually expressed in beats per
minute.

36. HTN is having blood pressure that is higher than


normal.

37. If something is found o/e, it was discovered during an


exam.
38. Rx is the specific drug or course of action prescribed to
treat a patient’s medical condition.

39. SOB is a condition in which a patient finds it more


difficult to breath than usual.

40. T  is a quantitative measurement of heat within the


body. It is can be used, in part, to gauge whether the body is
operating normally.

41. If a function is WNL , it is operating in a normal range.

42. XR is a visual image of all or part of the body acquired


with special equipment using electromagnetic radiation to see
bones and other internal aspects of the body.

43. to describe uncomfortable symptoms :  c/o

44. the amount of internal body heat measured :   T

45. Dx : "the identification of an illness or disease"   

46. the amount of force applied on blood vessel walls by


circulating blood : BP

47. the number of heartbeats in a given amount of time : HR

48. to be at an average level : WNL

49. discovered while investigating a patient’s health : o/e

50. The XR clearly showed that bone was broken.

51. The asthmatic patient complained of SOB

52. Rx for the infection included antibiotics


53. The patient with high blood pressure was diagnosed
with HTN

54. A  cc is a unit of volume equal to a cube whose sides are


equal to one centimeter

55. A gtt is a unit of liquid volume equal to the amount of


liquid which comes from a dropper, or about 1/12th of a
milliliter.

56. A g is a unit of mass which is equal to one-thousandth of


a kilogram

57. gtt (s) are drops of liquid administered to the eye.

58. A mcg is a unit of mass equal to one millionth of a gram.

59. A mEq is 1/1000th the weight of the minor component


of a chemical solution dissolved in the major component

60. A mg  is a unit of mass equal to one thousandth of a


gram.

61. A ml is a unit of liquid volume equal to one thousandth


of a liter and equal to one cubic centimeter.

62. A tbsp is a measure of volume equal to the amount a


standard tablespoon can hold or about three teaspoons.

63. A tsp is a measure of volume equal to the amount a


standard teaspoon can hold, or almost five milliliters.

64. Which of the following is equal to one ml?   1 cubic


centimeter

65. a unit of mass equal to one millionth of a gram : mcg

66. a unit of mass equal to one thousandth of a gram : mg


67. 1/1000th the weight of the minor component of a
chemical solution dissolved in the major component : mEq

68. a unit of mass which is equal to 1/1000th of a kilogram :


g

69. a measure of volume equal to the amount a standard


teaspoon can hold : tsp

70. a measure of volume equal to the amount a standard


tablespoon can hold or about three teaspoons : Tbsp

71. Please put 2 drop (s) of cleaning solution in each ear.


Use a dropper.

72. Half a liter is equal to 500 ml (s)

73. One thousand g (s) make up one kilogram

74. To administer medicine is to give it to a patient.

75. A(n) dosage is the correct amount and frequency of


medicine to give to a person.

76. A(n) IV is a method of administering medicine into a


vein using a syringe, often over a long period of time.

77. A(n) IM injection is a medicine that is injected into a


muscle with a syringe.

78. If medicine is given P.O., it is taken orally, or through the


mouth.

79. If a medicine is given P.R, it is taken through the rectum.

80. A route of administration is the path by which a


medicine is taken into the body.
81. If a medicine is SQ, it is injected into the fatty layer
under the skin with a syringe.

82. If a medicine is taken SL, it is given beneath the tongue

83. If a medicine is topical, it is applied to a certain part of


the surface of the body.

84. injected into the fatty layer under the skin with a
syringe  : subcutaneous

85. taken orally, or through the mouth : P.O

86. given beneath the tongue : sublingual

87. taken through the rectum : P.R

88. injection into a vein using a syringe, often over a long


period of time : IV

89. applied to a certain part of the surface of the body :


topical

90. Is the route of administration for this medicine


sublingual or P.O.?

91. Please get me a syringe so I can give this intramuscular


injection

92. How should we administer Mr. Smith’s medicine?

93. For this patient, the correct dosage is 200 milligrams


per day.

Tuầ n 2

94. If someone has a runny something, he or she has


experienced it regularly or repeatedly.
95. A(n) muscle ache is a pain felt in the muscles.

96. A(n) past medical history (PMH) is a patient's record of


previous illnesses, procedures, and other medical details.

97. Medication that is given at bedtime : qhs

98. To wheeze is to breathe with difficulty in a noisy


manner.

99. Medication that is given immediately  stat

100. If something is runny, it has liquid flowing or leaking


out of it.

101. A(n) headache is a pain felt in the head.


102. Medication that is given every hour : qh
103. Medication that is given four times per day : QID
104. A(n) social history is a patient's record of lifestyle and
personal details, such as occupation and marital status.

105. Medication that is given every other day  QOD


106. A(n) fever is an illness that causes body temperature to
rise,

107. A(n) allergy is a medical condition that causes a


reaction or illness when someone comes in contact with a
particular substance.

108. If a medication that is given twice per day : BID


109. If something is current, it is happening at the present
time
110. To throb is to have pain that comes and goes very
quickly.

111. To cough is to force air loudly through the throat


because of an illness or throat irritation.

112. A(n) symptom is a feeling or physical change that


indicates illness.

113. A(n) family medical history is a record of the medical


conditions of a patient's family that might affect the patient's
health.

114. A(n) procedure is a medical treatment performed by a


doctor or surgeon.

115. A(n) cold is an illness that can cause coughing, a runny


nose, and a sore throat.

116. A medication that is taken before meals  ac


117. A(n) complaint is pain or illness reported by a patient.
118. A(n) onset is the start or first instance of something.
119. Medication that is given as needed : PRN
120. data is a collection of information.
121. Medication that is given three times per day : TID
122. flu is a viral illness that can cause fevers, aches, and
wheezing,

123. Medication that is given after meals : pc


124. QH means given every hour
125. If something is current, it is happening at the present
time 

126. An illness that causes discomfort in the head and body   


: cold

127. Fatigue is a symptom _ of the flu 


128. the first instance of something : onset
129. The patient's past medical history included her
previous surgeries 

130. A(n) social history is a patient’s record of lifestyle and


personal details, such as occupation and marital status.

131. If a medication is given TID, it is given three times per


day.

132. A symptom is a feeling or physical change that indicates


illness.

133. A cold is an illness that can cause coughing, a runny


nose, and a sore throat.

134. If a medication is given stat, it is given immediately.


135. If a medication is given pc, it is given after meals.
136. According to the thermometer, the patient has a fever
137. If something is runny, it has liquid flowing or leaking
out of it.

138. The pain in my back throbs


139. TID means given three times per day
140. To cough is to force air loudly through the throat
because of an illness or throat irritation.

141. a pain or illness reported by a patient : complaint


142. If a medication is given ac , it is before meals.
143. flu  is a viral illness that can cause fevers, aches, and
wheezing,

144. The patient should take this medication before he eats.


The underlined part has the same meaning as: ac

145. To throb is to have pain that comes and goes very


quickly.

146. a medical treatment : procedure 


147. A(n) complaint is pain or illness reported by a patient.
148. If a medication is given qh, it is given every hour,
149. QID means: given four times per day
150. If a medication is given BID , it is given twice per day.
151. You should take this antibiotic when you go to bed. The
underlined part has the same meaning as: qhs

152. PRN means:  qhs


153. The patient's current condition was caused by a recent
injury.

154. A fever is an illness that causes body temperature to


rise,
155. If a medication is given QID , it is given four times per
day.

156. To wheeze is to breathe with difficulty in a noisy


manner.

157. A(n) procedure is a medical treatment performed by a


doctor or surgeon.

158. I need 50 cc's of lidocaine immediately! The underlined


part has the same meaning as: stat

159. If a medication is given QOD , it is given every other day.


160. The patient's social history included her occupation.
161. a record of a patient’s family’s conditions : family
medical history

162. Medical professionals take medical histories to uncover


information that might help with diagnoses.

163. to breathe noisily and with difficulty : wheeze


164. If a medication is given qhs, it is given at bedtime.
165. data  is a collection of information.
166. If a medication is given PRN, it is given as needed.
167. Paul's family has a history of cancer.
168. A(n) family medical history is a record of the medical
conditions of a patient’s family that might affect the patient’s
health.

169. If someone has a history of something, he or she has


experienced it regularly or repeatedly.
170. Take two of these after you eat. The underlined part has
the same meaning as: pc

171. Helen was coughing because of the flu


172. having liquid leaking from something: runny
173. A(n) allergy is a medical condition that causes a
reaction or illness when someone comes in contact with a
particular substance.

174. to force air loudly through the throat : cough


175. A(n) past medical history is a patient’s record of
previous illnesses, procedures, and other medical details.

176. You will need to take a pill once every hour until you
start to feel better : qh

Tuầ n 3

177. A(n) ultrasound is a medical imaging technique that


uses the reflection of sound waves to produce an image of the
body.

178. A(n) biopsy is a medical procedure in which a piece of


tissue is removed and examined to help determine an illness.

179. If something is renal, it is related to the kidneys.


180. blood pressure is a measure of the pressure with which
blood moves through the body.

181. medical imaging is the process of creating pictures of


the human body for the purpose of diagnosing and treating
medical problems.

182. A(n) endoscope is a thin, tubular instrument used to


examine the inside of an organ or body cavity.
183. To affect something such as mood is to bring about a
change in it.

184. A(n) pulse is a measure of heartbeats in a given period


of time. One way to take this measurement is to place the
fingers over a major artery in the neck, wrist, or other location
and press them against a bone to feel the palpations of the
heart as blood moves through the artery.

185. radiography is the use of x-rays to view images of the


internal human body.

186. creatinine is a waste product found in blood that the


kidney usually removes.

187. To evaluate something is to determine the qualities of


its condition or state.

188. body language is the conveyance of information about a


person's physiological or emotional state by the way he or she
moves.

189. To feed an endoscopic tube is to insert it into the body


in order to take internal pictures,

190. A(n) inspection is an organized examination of a


patient's physiological state as compared to what is
understood to be normal.

191. auscultation is the examination of something by


listening with or without an instrument such as a stethoscope.

192. palpation is the examination of something by touch.


193. A(n) observation is something that someone notices, or
the act of noticing something.

194. albumin is a type of protein found in the body.


195. vital signs are statistical measures of essential body
functions such as temperature, pulse rate, blood pressure, and
respiration.

196. A(n) pathology report is a report that discusses what


was found after cells and tissue were examined.

197. A(n) magnetic resonance imaging (MRI) is a medical


imaging technique that uses magnetic forces on atoms to
produce an image of the body.

198. A(n) x-ray is a form of radiation that can be used to take


pictures of the internal human body

199. A glomerular filtration rate test (GFR) test is a test to


determine how much kidney function a person has.

200. chronic kidney disease (CKD) is a medical condition in


which a person loses kidney function over time.

201. A(n) urinalysis is a test that examines a urine sample.


202. A blood urea nitrogen test (BUN) test is a test to
determine the amount of urea nitrogen in the blood.

203. gel is a semi-solid substance placed between the


patient's skin and an ultrasound probe.

204. A(n) electrocardiogram (ECG)is a measurement of the


electrical activity of the heart over a period of time.

205. percussion is the act of tapping on an area of the body


such as the chest or abdomen to determine the condition of the
underlying bone or tissues.

206. A(n) CT scan is a form of medical imaging that uses


many two-dimensional X-rays to create a three-dimensional
image of an object.
207. A(n) pulse is a measure of heartbeats in a given period
of time. One way to take this measurement is to place the
fingers over a major artery in the neck, wrist, or other location
and press them against a bone to feel the palpations of the
heart as blood moves through the artery

208. palpation  is the examination of something by touch


209. A(n) urinalysis is a test that examines a urine sample.
210. a waste product found in blood that the kidney usually
removes : creatinine

211. Get a(n) ECG of that patient’s heart activity.


212. Which of the following is not an aspect of checking vital
signs?  evaluating posture   (evaluating patient's mood /
observation of the patient's body language)

213. A blood urea nitrogen (BUN) test is a test to determine


the amount of urea nitrogen in the blood.

214. something is renal, it is related to the kidneys.


215. The nurse forgot to determine the quality of the
patient’s posture : evaluate

216. A(n) observation is something that someone notices, or


the act of noticing something

217. A(n) electrocardiogram (ECG)is a measurement of the


electrical activity of the heart over a period of time.

218. a medical imaging technique that uses the reflection of


sound waves to produce an image of the body".  ultrasound

219. a type of protein found in the body  : albumin


220. To evaluate  something is to determine the qualities of
its condition or state.

221. Which of the following is an advanced medical imaging


technique?    CT scan.      (ECG  / MRI / CT scan)

222. Which of the following is an aspect of checking vital


signs? auscultation

223. The doctor performed an investigation of the patient’s


ear.   inspection

224. A(n) CT scan is a form of medical imaging that uses


many two-dimensional X-rays to create a three-dimensional
image of an object.

225. People can have a relatively normal life with just one
kidney.

226. a thin, tubular instrument used to examine the inside of


an organ or body cavity : endoscope

227. A(n) endoscope is an organized examination of a


patient’s physiological state as compared to what is
understood to be normal.

228. a test that examines a urine sample : GFR test -


Glomerular filtration rate / BUN test Blood Urea Nitrogen

229. body language  is the conveyance of information about a


person’s physiological or emotional state by the way he or she
moves.

230. Which of the following is NOT an advanced medical


imaging technique?  X-ray

231. The bone is likely broken, but take a(n) X-ray to make
sure.
232. The doctor will feed a tube into the man’s chest to see
pictures with the endoscope.

233. We will remove some tissue from your liver during the
biopsy.

234. The patient’s back pain seemed to make a difference


upon her mood : affect

235. Which of the following is a physical examination


technique? Auscultation

Physical examination techniques: -   auscultation


-
palpitation
- percussion

236. Which of the following is an advanced medical imaging


technique? ECG

237. Apply this gel  to the area before using the ultrasound
machine.

238. To affect something such as mood is to bring about a


change in it.

239. Your blood pressure reading, at 110/65, is on the low


end of the normal range.

240. The use of X-rays to view images of the internal human


body : radiography

241. a medical condition in which a person loses kidney


function over time". chronic kidney disease

242. gel is a semi-solid substance placed between the


patient’s skin and an ultrasound probe.
243. The pathology report will show the results from several
tests.

244. A(n) endoscope is a thin, tubular instrument used to


examine the inside of an organ or body cavity.

245. A(n) pathology report is a report that discusses what


was found after cells and tissue were examined.

246. a test to determine the amount of urea nitrogen in the


blood : BUN test

247. vital signs are statistical measures of essential body


functions such as temperature, pulse rate, blood pressure, and
respiration.

248. Which of the following is an aspect of checking vital


signs?   checking pulse

249. radiography  is the use of x-rays to view images of the


internal human body.

250. CT scan is a form of medical imaging that uses many


two-dimensional X-rays to create a three-dimensional image of
an object"

251. A(n) magnetic resonance imaging (MRI) is a medical


imaging technique that uses magnetic forces on atoms to
produce an image of the body.

252. creatinine is a waste product found in blood that the


kidney usually removes.

253. Which of the following is an advanced medical imaging


technique?  MRI

254. Through watching carefully the doctor noticed that the


patient was limping : observation

255. A GFR test tests how well kidneys are working.


256. a yellow liquid waste product that the body produces :
urine

257. A(n) biopsy is a medical procedure in which a piece of


tissue is removed and examined to help determine an illness : 

258. What is one use for percussion techniques?  to check the


condition of internal organs

259. a medical imaging technique that uses magnetic forces


on atoms to produce an image of the body".  MRI

260. percussion is the act of tapping on an area of the body


such as the chest or abdomen to determine the condition of the
underlying bone or tissues.

261. Who is most likely to be examined by an ultrasound?   a


patient who is pregnant

262. Which of the following is an aspect of checking vital


signs?  taking temperature

263. A(n) ultrasound is a medical imaging technique that


uses the reflection of sound waves to produce an image of the
body

264. A glomerular filtration rate (GFR) test is a test to


determine how much kidney function a person has.

265. A(n) x-ray is a form of radiation that can be used to take


pictures of the internal human body

266. auscultation is the examination of something by


listening with or without an instrument such as a stethoscope.

267. If one or both kidneys decline in function you may have 


renal failure.
268. chronic kidney disease (CKD) is a medical condition in
which a person loses kidney function over time.

269. blood pressure is a measure of the pressure with which


blood moves through the body.

tuầ n  4

270. packaging is a material used to wrap or protect good


that are sold in stores

271. In Russia, we prefer to buy over-the-counter products,


like cold remedies or cough syrup, from people in pharmacies
wearing white lab coats

272. By the end of the meeting I hope we will have come up


with deliverables for getting the project off the ground and a
full to do list.

273. Laboratory technician operates complex scientific


instruments and performs tests to determine whether
ingredients in liquids, powders, or tablets meet requirements.

274. In Russia, we prefer to buy over-the-counter products,


like cold remedy or cough syrup, from people in pharmacies
wearing white lab coats.

275. Preclinical data is the information about a medication


that is assessed before clinical trials.

276. With your input, I'll be able to finalize the timelines for
planning and implementation and decide on milestone (s)
before our next meeting.

277. Prescription drug is the medicine bought in a pharmacy


and requiring a written note from the doctor.

278. Feasibility study is an investigation to determine the


advantages, practicality, and profitability of a proposed project
279. With your input, I'll be able to finalize the timelines for
planning and implementation and decide on milestones before
our next meeting.

280. I operate complex scientific instruments and perform


tests to determine whether ingredients in liquids, powders, or
tablets meet requirements.

281. Feasibility study is an investigation to determine the


advantages, practicality, and profitability of a proposed project.

282. It's the Medical writer job to research, write, and edit
clinical and study reports before the pharmaceutical company
submits them to regulatory authorities.

283. In Europe, the strength of medicine varies considerably


depending on what health authorities allow.

284. I collect drug safety information about patients on our


medication (s).

285. I am the clinical trial manager assigned to this project


and am supported by two clinical research associates who will
work with test centres in northern Italy and in Slovenia

286. When people  liaise  with another, they work together


and keep each other informed about what is happening.

287. Unlike in many countries, you'll also find many cheerful


bright coloured ads in magazines, which promote anti-
depressants and other prescription drugs in the US.

288. Self-medicate means to take medicine without


consulting a physician.

289. Charley is to describe the technical equipment needed


with a cost estimate by the end of the month.

290. Regulatory Affairs department compiles the drug


documentation and submits it to the drug regulatory
authorities so the company can get authorization to market the
product.

291. Colleague is someone you work with; a co-worker


292. powder a dry substance in the form of very small grains.
293. In France, medicines should not only cure a disease, but
also look fresh and interesting.

294. A Formulation scientist develops pharmaceutical


dosage forms.

295. consultant is someone whose job is to give advice on a


particular subject.

296. A  Subsidiary  is a company which is part of a larger and


more important company.

297. Research and Development (R&D) department finds


new substances to make new drug formulations or changes
existing dosage forms, for example, from tablets to capsules.

298. I operate complex scientific instruments and perform


tests to determine whether ingredients in liquids, powders, or
tablets meet requirements.

299. Feasibility study is an investigation to determine the


advantages, practicality, and profitability of a proposed project.

300. Since the conclusion of our successful feasibility study,


we have also obtained very encouraging preclinical data.

301. Project members from Marketing, Production, and


Clinical Affairs are already on board

302. I would like you to introduce yourselves and say


something about your professional background, area of
expertise 
303. Analgesic is a medication to reduce or eliminate pain.
304. B.S stands for bachelor's degree.
305. Ingredient  is a substance in a drug.
306. We plan to launch our new drug in Europe first and to
apply for Food and Drug Administration (FDA) approval in the
US the following year.

307. CRO is searching for omeone to co-ordinate and


perform analytical testing for stability studies of new products.

308. We will need to fill the position of clinical trial manager


shortly. I'd appreciate it if you could write up a job
advertisement with the input below and place it in the
pharmaceutical journal we normally use.

309. Pharmaceutical companies must report serious adverse


events to the health authority

310. Pharmaceutical products in the pipeline are future


drugs, not yet on the market.

311. I was involved in the initial conceptual design phase, the


planning and building of our new pharmaceutical facility in
Shanghai, and now I am the plant manager.

312. We test or organize testing on live subjects and make


sure that our drugs are safe and effective for the patients.

313. Cross-cultural means involving two or more different


cultures.

314. Marketing and Sales department plans the promotion


and distribution of drugs which will be launched, and makes
decisions about the packaging or tablet colour of new products.
315. Clinical research associate performs clinical trials.
Clinical research associate  must also summarize, interpret and
process clinical data.

316. MSc stands for master of science degree.


317. We plan to launch all of these products in Europe first
and to apply for food and drug administration (FDA) approval
in the US the following year.

318. clinical research organization (CRO)  is an organization


that provides support to the pharmaceutical, biotechnology,
and medical device industries in the form of research services
outsourced on a contract basis.

319. Formulation scientists develop pharmaceutical dosage


forms.

320. According to European law, a qualified person is


responsible for the quality of each product that leaves the
production line

321. Production department compounds the raw materials


into drugs, packages them, and puts in the leaflets for the
patients.

322. Pharmaceutical companies must report serious adverse


events to the health authorities.

323. You need to be able to write scientifically and


technically accurate protocols in English.

324. A project manager co-ordinates and manages the cross-


functional teams that develop and launch a new product

325. As far as Marketing is concerned, Carole Marks will be


flying in from France. She'll give us more information on the
marketing claim (s) and a target patient profile.

326. Feasibility study is an investigation to determine the


advantages, practicality, and profitability of a proposed project.
327. A(n) memo is a short official note that is sent by one
person to another within the same company or organization.

328. Unlike in many countries , you'll also find many


cheerful, bright coloured ads in magazines, which promote
anti-depressant and other prescription drugs in the US.

329. The marketing department plans the promotion and


distribution of drugs which will be launched, and make
decisions about the packaging or tablet colour of new products

330. Quality is important all over the world, but in Japan we


take it one step further. We will reject a whole shipment of
drugs if we find the smallest scratch or imperfection in one
single package, even if it makes no difference to the product at
all.

331. BSc  stands for bachelor of science degree.


332. A  Pharmacovigilance manager  collects drug safety
information after approval and reports any serious adverse
events to the health authorities.

333. Some companies are successful at marketing their drugs


all over the world without making any major changes to them.
Others have different formulations, advertising, and packaging
in each country, due to differences in custom  (s) and laws.

334. Feasibility study is an investigation to determine the


advantages, practicality, and profitability of a proposed project.

335. Clinical Affairs  department tests or organizes testing on


live subjects, and makes sure that the drugs are safe and
effective for the patients.

336. Formulation scientists develop pharmaceutical dosage


forms.

337. I did research on clinical methodology


338. deadline  a date or time by which you have to do or
complete something.

339. MS stands for master's degree.


340. A Project manager  co-ordinates and manages the cross-
functional teams that develop and launch a drug.

341. Since the conclusion  of our successful feasibility study,


we have also obtained very encouraging preclinical data (=
end)

342. Quality Assurance (QA)  department ensures that


products meet the standards which the law requires, and
contain the active ingredients advertised.

343. A  Qualified person is personally responsible for the


quality of each product that leaves the production line. A
Qualified person must manage all the processes in production,
QA, and the labs to make sure SOPs are followed.

344. Before they become fully qualified, pharmacists in the


US have to take an examination to get a licence  to practise
pharmacy.

345. Regulatory affairs department compiles the drug


documentation and submits it to the drug regulatory
authorities so the company can get authorization to market 
the product

346. I received my master's degree at New York University


and licence to practise pharmacy in the United States

347. A  clinical trial manager  is a key position in the


management of clinical trials. He is responsible for managing
the clinical trial process by implementing effective strategies
for his/her organization.

348. Health regulations are rules or laws about health.


349. We compile the drug documentation and send it to the
regulatory drug authority so we can get authorization to
market the product.

Tuầ n 5

350. Medicine needs to be easily accessible. This is, of course,


a question of public health. On the other hand, these same
products can do harm if used incorrectly. This danger must be
avoided.

351. Scientists have made a major breakthrough in the


treatment of cancer.

352. When someone has palpitations, their heart beats very


fast in an irregular way. (conditions of heart racing )

353. Formulation is a mixture of ingredients prepared in a


certain way and used for a specific purpose.

354. Diabetes refers to a group of diseases that affect how


your body uses blood sugar (glucose).

355. The science of poisons, including their source, chemical


composition, action, tests , and even their antidote (s) , is what
we call Toxicology

356. Medication must meet four criteria in order to obtain


the status of a non-prescription or OTC. It must have: a large
margin of safety ,  low incidence of side effects, low potential
for misue and abuse, and labelling that provides adequate
directions for sale and effective use.

357. When substances are taken with alcohol or antibiotics,


their chemical form could change and even cause harmful  side
effects.

358. Solution is a liquid in which another substance has been


dissolve (d)
359. Research is the process of testing chemical compounds,
with the goal of finding a substance which has a beneficial
effect  on a targeted disease.

360. Nausea is the condition of feeling sick and the feeling


that you are going to vomit.

361. Suppository is a solid medicine which melts slowly in


the rectum or vagina.

362. Oral drops  are liquid preparations for oral use that are
intended to be administered in small amount with the aid of a
suitable measuring device.

363. When you chew food, you use your teeth to break it up
in your mouth so that it becomes easier to swallow.

364. Lotions are fluid preparations (aqueous) for external


application without friction.

365. Clinical trial is a scientific study designed to


systematically test a medical intervention in humans.

366. New chemical entity is a unique, pharmacologically


active product that has never previously been synthesized or
used to treat disease.

367. Ointments are semi-solid, smooth greasy preparations


for application to the skin for healing.

368. If you have Indigestion, you have pains in your stomach


and chest that are caused by difficulties in digesting food.

369. Dosage is the amount and frequency of a medicinal drug


that may be taken safely.

370. One of criteria to obtain the status of OTC product in the


US is that a medication must have low incidence of side effects.
371. In the fields of medicine, biotechnology and
pharmacology, drug discovery is the process by which new
candidate medications are discovered.

372. anaemia is a medical condition in which there are too


few red cells in your blood, causing you to feel tired and look
pale.

373. First in-man study is Phase-1 study in which a test


product is administered to human beings.

374. Some medications are available in liquid form, such


drops or syrup.

375. Pharmaceutical product labelling must provide


adequate directions for sale and effective use.

376. Dosage form is the final form of the medicine, e.g.


Tablet, powder, gel, spray, etc.

377. Toxicity is the degree to which a substance (a toxin or


poison) can harm humans or animals.

378. Pneumonia is the inflammation of the lungs. The lungs


become filled with liquid which makes it difficult to breathe.

379. Allergic reaction is the body's exaggerated immune


response to an internal or surface agent.

380. Oral solution is a liquid in which another substance has


been dissolved.

381. Toxicology is the study of poisons.


382. Pill is a small, round piece of medicine to be swallowed
without chewing.

383. An Inhaler is a small device with medicine to breathe in


through the mouth.
384. Suppository is a solid medicine which melts slowly in
the rectum or vagina.

385. A specialist or  expert  in the scientific field of chemistry


is called a chemist.

386. Which of the following dosage form(s) do the patients


favour (= prefer)?

387. Mensamint is a new dosage form of Mensadent. Known


side effects often include loss of sleep if taken in the late
afternoon or evening. occasionally (now and then ), an increase
in blood pressure may occur.

388. Dose  is the amount of substance given at one time.

389. Toxicology is the study of poison.


390. If a wound or a part of your body becomes septic , it
becomes infected.

391. Nasal spray is a substance dispensed as a fine spray


from a container into the nostril.

392. Soft gelatin capsule is a type of capsule that is usually


used to contain oils and for active ingredients that are
dissolved or suspended in oil.

393. If you have a fever when you are ill, your body
temperature is higher than usual.

394. Someone who suffers from insomnia finds it difficult to


sleep.

395. Syrup is a sweet, liquid medicine taken with a spoon or


cup.
396. Research is the process of testing chemical compounds,
with the goal of finding a substance which has a beneficial
effect on a targeted disease.

397. An Ailment is an illness, especially one that is not very


serious.

398. Pharmacology is the study of drugs, how they work, and


what they do in the body. Pharmacology can be divided into
two separate areas: Pharmacodynamics and Pharmacokinetics.

399. Asthma is a lung condition which causes difficulty in


breathing.

400. Medication must meet four criteria in order to abtain


the status of a non-prescription or over-the counter (OTC)
product. It must have: a large margin of safety, low incidence of
side effects, low potential for misuse and abuse, and - labelling
that provides adequate directions for sale and effective use.

401. Eye drops are a kind of medicine that you put in your
eyes one drop at a time.

402. Suppository is a solid medicine which melt (s) slowly in


the rectum or vagina.

403. Pharmacodynamics is the study of physiological effects


of drugs and the mechanisms of their actions (what the drug
does to the body)

404. Sublingual tablet is administered by placing it under the


tongue.

405. Lozenge is a solid preparation that is intended to


dissolve or disintegrate slowly in the mouth (e.g.. Sore throat)

406. Hard gelatin capsule is a type of capsule that is usually


used to contain medicine in the form of dry powder or very
small pellets.
407. Chewable tablet is chewed prior to swallowing. It is
designed for administration to children e.g. vitamin products.

408. Topical dosage forms are applied to the skin surface.


409. A Chronic illness or disability lasts for a very long time.
Opposite to acute.

410. Mensamint is a new dosage form of Mensadent. Known


side effects often include loss of sleep if taken in the late
afternoon or evening. Occasionally, an increase in blood
pressure may occur.

411. Diarrhoea is a condition in which faeces are discharged


from the bowels frequently and in a liquid form.

412. Bioavailability is the proportion of a drug or other


substance which enters the circulation when introduced into
the body and so is able to have an active effect.

413. Over-the-counter drug is a product which can be sold


without the patient seeing a doctor.

414. Effervescent tablet  is an uncoated tablet containing


substances that react in the presence of water and give off
carbon dioxide.

415. Patch is a medication on material or cloth placed on the


skin.

416. Toxicologist is an expert in the science of poisons.


417. Drug development is the process of carry forward
scientific discoveries made during the research process, with
the goal of producing a marketable drug.

418. Development is the process of carrying forward


scientific discoveries made during the research process, with
the goal of producing a marketable drug
419. Chemist is an expert in chemistry. In the UK, this word is
also used for the person who prepares and sells medicine, also
known as a pharmacist in the US.

420. Pharmacokinetics is the study of the bodily absorption,


distribution, metabolism, and excretion of drugs (what the
body does to the drug)

421. Route of administration is the path by which a drug,


fluid, poison, or other substance is taken into the body.

422. Gel is a drug delivery system consisting of a semi-solid,


jelly-like substance.

423. An inhaler is an aerosol dispensing device which


releases medication into the mouth of the patient.

424. Behind-the-counter medicine can be purchased without


a prescription but only with the personal involvement of a
pharmacist.

425. Tablet is a hard, compressed medication in round, oval


or square shape

426. We will have to test the bioavailability to be able to


calculate dosages for non-intravenous routes of drug
administration for this NCE.

427. Mensamint is a new dosage form of Mensadent (


Obtainable with plysician's prescription only)

428. Chemists and pharmacologist (s) are also interested in


how the medicine is administered, so they often ask about its
formulation.

429. aerosol is a container with a liquid that is administered


in spray form.

430. Bronchitis is the inflammation of the bronchial tubes,


characterized by coughing, difficulty in breathing.
431. Patches are easy to apply, not too expensive, and can be
placed right at the point of pain.

432. Toxicology is the science of poisons, including their


source, chemical composition, action, tests and their antidotes.

433. One of criteria to obtain the status of OTC product in the


US is that a medication must have low potential for misuse and
abuse.

434. OTC Pharmaceutical products must have labelling that


provides adequate directions for sale and effective use.

435. Liniment is an oily liquid to rub on painful body parts to


reduce pain.

436. At present, the Food and Drug Administration is


reviewing its current policy on the number of categories of
medicines.

437. In Canada, Behind-the-counter medicines are those that


a patient can obtain without a prescription, but only with the
personal involvement of a pharmacist.

438. Inhaled dosage forms are breathed in through mouth or


nose and are often used to treat respiratory diseases.

439. Time-release delivery means a drug preparation that


gradually releases an active substance over a period of time.

Tuầ n 6

440. GCP stands for Good Clinical Practice.


441. All operational procedures and methods must also be
inspected for accuracy.

442. Contaminated products are no longer pure and


acceptable for sale or public use and, therefore, must be
returned to the manufacturer or destroyed.
443. improper disposal of toxic waste material was recorded.
(= incorrect/ wrong)

444. The reason for interim testing, or Product sampling, is


to check the quality of pharmaceutical products.

445. Protective glasses/ goggles must be worn at all times in


the laboratory.

446. Although there were no serious instances of non-


compliance, a number of incidents of undesirable conditions
and practices were observed. These need to be corrected
before the follow-up review in 30 days

447. Proper protective clothing and safety equipment must


be worn at all times

448. Endpoint testing is carried out at the end of every


manufacturing process. This is to ensure that all procedures
have been performed in compliance with industry and
company standards.

449. documentation is important and necessary at every step


of the processes, activities, and operations involved in drug
manufacturing.

450. A/An auditor inspects and verifies the safety


procedures in the lab.

451. This memo is to advise you that your department has


been scheduled for a periodic audit of the laboratory safety
systems and procedures.

452. Standard operating procedures (SOPs) are written and


used by companies to make it easier for them to follow GxP.
These are a set of written instructions to maintain
performance and results

453. CAPA focuses on the systematic investigation of non-


conformance events (errors or deviations), to prevent their
occurrence (for preventive action) or recurrence (for
corrective action).
454. Documentation is important and necessary at every
step of the processes, activities, and operations involved in 
drug manufacturing.

455. I suggest you dispose of toxic waste in the bins provided


for this purpose.

456. Please confirm receipt of this memo and send us a copy


of all your correspondence with regard to this scheduled audit.

457. According to reports, it seems that an unanticipated


reaction between the drug's active ingredient and the
chemicals used as part of the cleaning processes at the site was
the cause of the contamination.

458. At the end of every stage of a product's manufacturing


process,  Endpoint testing  is done to maintain quality
standards.

459. Endpoint testing is carried out at the end of every


manufacturing process to ensure that all procedures have been
performed in compliance with industry and company
standards.

460. Any observation or finding noted by the auditors is


categorize (d) as either major, minor, or critical.

461. Quality control involves interim and product sampling


procedures, which are carried out to check product quality.

462. If any  non-compliance is observed during the audit, the


department will be informed so they can take corrective action.

463. A product recall took place following reports from


patients that their medication had a strange odour. Several
patients from a number of different countries made the
complaint  within a short period of time.

464. Corrective Action/Preventive Action (CAPA) is a part of


the overall Quality Management System (QMS) required for
GMP. It focus (es) on the systematic investigation of non-
conformance events (errors or deviations), to prevent their
occurrence (for preventive action) or recurrence (for
corrective action).

465. Even a product that has been marketed for years might
have to be taken off the market in a Product recall if serious
adverse reactions occur.

466. GDP stands for Good Documentation Practice


467. proper documentation not only enables traceability, but
also allows a complete product recall from the market, if
necessary.

468. To ensure that laboratory workers are asked certain


questions about safety procedures, auditors use a Checklist

469. Corrective action / Preventive action ( CAPA ) is a part


of the overall Quality Management System ( QMS) required for
GMP .

470. Aspirin mainly used for pain relief and fever.


471. Standard operating procedures (SOPs) are a set of
written instructions to maintain performance and results. They
are the basis of good QA and QC system.

472. Proper protective clothing and safety equipment must


be worn at all times.

473. A few years ago, a well-known European


pharmaceutical company was forced to recall one of its drugs
due to claim s of product contamination.

474. Validation of cleaning processes is essential in this


industry, because chemical or bacterial contamination of drug
products can potentially lead to severe public health risks.

475. A(n) annual audit of safety procedures in all


laboratories is carried out yearly.

476. Corrective action prevents recurrence of errors


477. Standard operating procedures (SOPs) are written and
used by companies to make it easier for them to follow GxP
These are a set of written instructions to maintain
performance and results

478. Disinfectant must be used on all equipment following an


experiment  with laboratory animals.

479. Even a product that has been marketed for years might
have to be taken off the market if serious adverse drug reaction
(s) occur.

480. Special containers are provided for the disposal of toxic


waste materials.

481. An internal audit involes inspection and validation of


operational methods, procedures, equipment to ensure
functionality, accruacy and validity

482. Any observation or Finding noted by the auditors is


categorized as either major, minor, or critical.

483. Beyond the filed of manufacturing, good practice must


be adhere (ed) to in all processes in a pharmaceutical company

484. The goal of an internal audit is to identify any areas


requiring corrective or preventive actions. It is done to assure
compliance with industry standards, especially for safety
procedures.

485. The quality assurance process in good manufacturing


practice (GMP) includes product quality control, sampling, and
testing.

486. It is absolutely essential to move lab mice outdoors in


closed cage (s) .

487. Special container (s) are provided for the disposal of


toxic waste materials.

488. Preventive action prevents occurrence of errors.


489. Manufacturing processes and procedures must go
through periodic  Validation to guarantee that they are still of
an acceptable standard.

490. disinfectant must be used on all equipment following


any experiments with laboratory animals.

491. Inspection and validation are required to prove that the


manufacturing and testing equipment is functional.

492. An Odour is a distinctive unpleasant smell.


493. All operational methods and procedures must also be
inspected for accuracy.

494. A well-known European pharmaceutical company was


force (ed) to recall one of its drugs due to claims of product
contamination.

495. GAP stands for Good Auditing Practice.


496. Proper documentation not only to enable (s)
traceability, but also allows a complete product recall from the
market.

497. A/an fire blanket is a safety device consists of a sheet of


a fire retardant material which is placed over a fire in order to
extinguish it.

498. The reason for interim testing, or product sampling, is


to check the quality of pharmaceutical products

499. The documentation required for all research processes


and development steps ensures the Traceability of a drug.

500. Auditors generally watch or observe safety procedures


in the lab.

501. Lab animals must be transported in covered cages.


502. Endpoint testing is carried out at the end of every
manufacturing process. This is to ensure that all procedures
have been performed in compliance with industry and
company standards.

503. All laboratory work must be documented in accordance


with GLP.

504. Preventive action prevents occurrence of errors


505. Quality assurance involves all manufacturing processes
in GMP which make sure the goods produced are kept at high
standards.

506. GLP stands for Good Laboratory Practice.


507. CAPA stands for Corrective Action/Preventive Action. It
is a part of the overall Quality Management System (QMS)
required for GMP

508. All work with virus- infected animals must be


performed in the bio-safety cabinet.

509. Small biological agent spills must be covered with a


paper towel and treated with bleach .

510. GSP stands for Good Safety Practice


511. Safety procedures make sure that the health and well-
being of laboratory workers are guaranteed.

512. advance notice of this meeting was very short.


513. Small biological agent spills must be covered with a
paper towel and treated with bleach .

514. A Holistic approach looks at all aspects of a


pharmaceutical company together to make sure that the entire
process meets high industry standards.
515. A few years ago, a well-known European
pharmaceutical company was forced to recall one of its drugs
due to claims of product contamination. The drug
manufacturer was unable to say just how many patients were
taking this drug at the time. However, it estimated the global
figure at over 40,000 people.

516. A/an Gas mask is a device that you wear over your face
in order to protect yourself from poisonous gases.

517. beyond the field of manufacturing, good practice must


be adhered to in all processes in a pharmaceutical company. No
process can be considered isolated from the others.

518. An internal Audit involves inspection and validation of


operational methods, procedures, equipment to ensure
functionality, accuracy and validity.

519. GMP stands for Good Manufacturing Practice.


520. The company claims that a cleaning error was the
reason for the entire incident. This clearly underlines the
danger  of underestimating the importance of the cleaning
process in pharmaceutical manufacturing.

521. Toxic or hazardous materials must be disposed of


properly.

522. Scientists often read journals and go to international


conferences, because they need to stay up-to-date in their
scientific fields.

523. You need to disinfect all equipment following any


experiments with laboratory animals.

524. Contaminated products are no longer pure and


acceptable for sale or public use and, therefore, must be
returned to the manufacturer, or destroyed.

525. A few years ago, a well-known European


pharmaceutical company was forced to recall one of its drugs
due to claims of product contamination
526. Contaminated drugs are no longer pure and acceptable
for sale or public use and, therefore, must be returned to the
manufacturer, or destroyed.

527. inspection and validation are required to prove that the


manufacturing and testing equipment is functional

528. Please confirm receipt of this memo and send us a copy


of all your correspondence with regard to this scheduled audit.

529. Documentation is important and necessary at every


step of the processes, activities, and operation (s) involved in
drug manufacturing.

530. We should tell the lab staff to double-check that all the
labs are spotlessly clean and that all lab devices and equipment
are where they should be - at every single workstation.

531. Quality Management System (QMS) is a formalized


system that documents processes, procedures, and
responsibilities for achieving quality policies and objectives.

532. A well-known European pharmaceutical company was


forced to recall one of its drugs due to claims of product
contamination.

533. Corrective Action/Preventive Action (CAPA) focuses on


the systematic investigation of non-conformance events
(errors or deviation (s)), to prevent their occurrence (for
preventive action) or recurrence (for corrective action).

534. Overshoes are shoe covers used to reduce foot borne


contamination and help maintain a sterile environment.

535. Eye bath is a/an apparatus to wash the eyes after


exposure to chemical contamination.

536. The quality assurance process in good manufacturing


practice (GMP) includes product quality control, sampling, and
testing.
537. Endpoint testing is carried out at the end of every
manufacturing process. This is to ensure that all Procedure (s)
have been performed in compliance with industry and
company standards.

538. To clarify something means to make it easier to


understand, usually by explaining it in more detail.

539. Genotoxic substance is a chemical that damages cellular


DNA, resulting in mutations or cancer.

Tuầ n 7 

540. in vitro means "in cells in a test tube"


541. During the preclinical developmentof a drug ,
laboratory tests document the effect of the investigational drug
in living organism , and in cells in a test tube (in vitro).

542. Phase III Trials: A large group of patients is studied and


closely monitored by physicians for efficacy and any adverse
events after long-term exposure to the drug.

543. Adverse reaction refers to all abnormal and unintended


response to an investigational medicinal product related to any
dose administered.

544. cancer is a serious disease in which cells in a person's


body increase rapidly in an uncontrolled way, producing
abnormal growths.

545. A drug that is intended to act on the sinuses may be


formulated as a time-release capsule, or as a nasal spray.

546. Creams are semi-solid emulsion, that is mixtures of oil


and water.

547. The parents took the authority to court after their


daughter had died of cancer.
548. Adverse reaction refers to all abnormal and unintended
responses to an investigational medicinal product related to
any dose administered.

549. Do terminally ill patients have the legal right to try to


prolong their lives by taking experimental drugs?

550. The safety and efficacy of a drug can only be determined


by conducting rigorous clinical trials, according to the FDA.

551. In Phase III, a large group of patients is studied and


closely monitored by physicians for efficacy and any adverse
events after long-term exposure to the drug.

552. In phase Phase IV , further information regarding drug's


safety, efficacy, and the ideal(optimal) use of the drug is
collected.

553. In the preclinical stage of drug development, a(n)


investigational drug must be tested extensively in the
laboratory. This is to ensure it will be safe to administer to
humans.

554. in vivo means "in living organisms"


555. In Phase I the drug reacts in the body, toxicity,
metabolism, absorption, and excretion are observed and
documented.

556. Phase I Trials: These are studies which are performed to


evaluate the safety of drugs in healthy people, and to
determine the pharmacological properties of drugs.

557. Phase IV is the post-marketing study after getting


approval for general sale.

558. Phase II is the first phase in which patients with the


target disease or disorder take part.
559. Phase I Trials: These are studies which are performed to
evaluate the safety of drugs in healthy people and to determine
the pharmacological properties of drugs.

560. Phase I is performed to evaluate the safety of drugs in


healthy people, and to determine the pharmacological
properties of drugs

561. Clinical trials are mainly aimed at answering scientific


questions. In general, their goal is to gather statistics to
determine whether an experimental drug is safe and effective.

562. After gaining evidence that the drug is effective, these


controlled and uncontrolled trials are carried out to obtain
additional information to evaluate the overall benefit-risk
relationship of the drug.

563. The parents of a 21-year-old woman challenged the


FDA.They took the authority to court after their daughter had
died of cancer.

564. In the preclinical stage of drug development, an


investigational drug must be tested extensively in the
laboratory. This is to ensure it will be safe to administer to
humans.

565. CMC stands for Chemistry, Manufacturing and Controls.


It is a part of new pharmaceutical product application to the US
Food and Drug Administration.

566. The dogs started retching and vomiting and were


separated to allow closer observation.

567. An adverse event is any abnormal medical occurrence in


a patient or clinical trial subject after a medicinal product has
been administered .

568. Phase IV Trials: They are carried out in order to gather


further information about the drug's safety, efficacy, and
optimal use.
569. Sensitive means quick to detect or respond to slight
changes, or influences. e.g. Dogs are more Sensitive to drugs
than mini-pigs.

570. An adverse event is any abnormal medical occurrence in


a patient or clinical trial subject after a medicinal product has
been administered.

571. Test subjects in the treatment group receive the


medication under study, whereas the control group receives
either a standard medication or a placebo.

572. Phase III is the final phase before getting marketing


approval.

573. Extensive documentation must be provided to the


appropriate regulatory authorities.

574. Sensible means practical and reasonable. e.g. It was a


Sensible decision to cancel the trial.

575. Regulatory agencies require testing that documents the


characteristics -chemical composition,purity quality,and
potency -of thedrug's active ingredient,and of the formulated
drug.

576. A Chemistry lab technician assists chemists and


chemical engineers using chemicals and related products

577. Shortly means 'soon'. e.g. The adverse event occurred


shortly after the injection.

578. Drug Excretion is the removal of a drug or its


metabolites from the body.

579. Phase II clinical trial is performed after there is


preliminary evidence that the drug is effective.

580. Phase III is the final phase before getting marketing


approval.
581. The products of drug metabolism are called Metabolites.
582. Briefly means 'for a short time' . e.g. The trial director
spoke briefly to his staff about the current status of the trial.

583. Miki has been invited to join an impromptu lab meeting


about drug substance MPP 010098, which is being tested in
dogs. ( = without planning or organizing it in advance.)

584. The general health and behaviour of the dogs were


checked twice a day.

585. Phase II Trials: These are controlled studies conducted


to evaluate the effectiveness of the drug in a particular
indication and to determine possible side effects and risks

586. Regulatory agencies have to give permission to


commence with the clinical testing in humans, which is also
done at our company.

587. The general health of the dogs was regularly checked.


On Day 2, abnormalities regarding food consumption were
observed shortly after administration in the high-dosegroup.

588. In addition, the overall appearance and behaviour of


each animal was assessed twice a day

589. Effect is the result of a change. e.g. I felt the Effect of the
new ointment right away.

590. An adverse event is any abnormal medical occurrence in


a patient or clinical trial subject after a medicinal product has
been administered. It does not necessarily have a causal
relationship with the medicinal product.

591. An Adverse event is any abnormal medical occurrence


in a patient or clinical trial subject after a medicinal product
has been administered. It does not necessarily have a causal
relationship with the medicinal product.
592. Many terminally ill people fall victim to the therapeutic
misconception that the objective of trials is to cure them.

593. In phase Phase II, testings are done to determine the


safety and efficacy of the drug in treating the condition and
establishes the minimum and maximum effective dose.

594. Preclinical studies refer to the testing of an


investigational drug, a procedure, or another medical
treatment in the laboratory to ensure it will be safe to
administer to humans. (also called preclinical development)

595. abnormality (s) regarding food consumption were


observed shortly after administration in the high- dose group.

596. Phase II Trials are controlled studies conducted to


evaluate the effectiveness of the drug in a particular indication
and to determine possible side effects and risks.

597. The results of all testing must be provided to the FDA in


the United States and/or other appropriate regulatory agencies
in other countries in order to obtain permission to begin
clinical testing in humans.

598. Drug Absorption is the movement of a drug from its site


of administration into the blood.

599. Subjects in a trial must be willing to be randomly


assigned to either the group which receives the unapproved
medication or the one which gets a placebo

600. Phase III is the final phase before getting marketing


approval.

601. The safety and efficacy of a drug can only be determined


by conducting rigorous clinical trials, according to the FDA.

602. Many terminally ill people fall victim to the 'therapeutic


misconception that the objective of trials is to cure them.
603. First of all, it is the intention of the company to
complete the preclinical trials by the end of the year.

604. A Disease is an abnormal condition that affects the body


of an organism, often caused by pathogens. e.g. There is a
history of lung Disease in the family.

605. The active ingredient currently being tested seems to


affect the kidneys.

606. Illness is used to describe a person who is in a poor


state of health. e.g. He missed five days of work because of
Illness.

607. Toxicology ís the study of the potential risks to the body.


608. A Control group in preclinical studies is a group of test
animals that is not exposed to the medication under study. In
an experiment, this group is treated just like the other animals,
but does not receive the active ingredient. This group is then
compared with the treated animals in order to validate the
results of the test.

609. Drug Distribution is the movement of drugs throughout


the body after absorption.

610. The results of all testing must be provided to the FDA in


the United States and/or other appropriate regulatory agencies
in other countries in order to obtain permission to begin
clinical testing in humans.

611. Phase II is performed after there is preliminary


evidence that the drug is effective.

612. Low-dose/mid-dose/high-dose groups are three groups


of animals which receive different concentration (s) of the
medication understudy.

613. A Biology lab technician works with living organisms.


614. Phase III is performed after there is preliminary
evidence that the drug is effective to obtain additional
information to evaluate the overall benefit-risk relationship of
the drug.

615. Drug Metabolism describes the chemical reactions


catalysed by enzymes that change drugs into compounds
which are easier to eliminate.

616. take part is the first phase in which patients with the
target disease or disorder.

617. The active ingredient can be tested in humans only after


these tests have been successfully completed and authorization
has been given.

618. Drug absorption is the movement of a drug from its site


of administration into the blood.

619. Drug metabolism describes the chemical reactions


catalysed by enzymes that change drugs into compounds
which are easier to eliminate.

620. Drug distribution is the movement of drugs throughout


the body after absorption.

621. Adverse reaction refers to all abnormal and unintended


responses to an investigational medicinal product. It is related
to the dose administered

622. An adverse event is any abnormal medical occurrence in


a patient or clinical trial subject after a medicinal product has
been administered. It does not necessarily have a causal
relationship with the medicinal product.

623. Side effect is any unintended reaction caused by a drug


or medical treatment. This term is used by the general public,
but is often avoided by medical authorities

624. The active ingredient currently being tested seems to


affect the kidneys.
625. A chemistry lab technician assists chemists and
chemical engineers using chemicals and related products

626. A biology lab technician works with living organisms


627. A control group in preclinical studies is a group of test
animals that is not exposed to the medication under study. 

628. A control group in preclinical studies is a group of test


animals that is not exposed to the medication under study

629. in vivo studies that are conducted on whole, living


organisms, usually animals, including humans, and plants as
opposed to a partial or dead organism.

630. In vivo studies that are conducted on living organisms 


631. During the preclinical development of a drug,
laboratory tests document the effect of the investigational drug
in living organisms (in vivo), and in cells in a test tube (in vitro)

632. The results of preclinical testing are used by experts in


pharmaceutical methods to determine how to best formulate
the drug for its intended clinical use

633. The results of all testing must be provided to the FDA in


the United States and/or other appropriate regulatory agencies
in other countries in order to obtain permission to begin
clinical testing in humans.

634. The results of all testing must be provided to the MHRA


in the United Kingdom and/or other appropriate regulatory
agencies in other countries in order to obtain permission to
begin clinical testing in humans.

635. First of all, it is the intention of the company to


complete the preclinical trials by the end of the year.
636. Regulatory agencies have to give permission before
clinical testing can be conducted in humans.

637. Extensive documentation must be provided to the


appropriate regulatory authorities.

638. A drug intended to act on the skin can be formulated as


a cream.

639. The requirements of drug bioavailability determine how


it will be administered to humans.

640. Could somebody please fill me in on what the problem


is ? 

641. Phase I trials are studies which are performed to


evaluate the safety of drugs in healthy people and to determine
the pharmacological properties of drugs

642. Phase II trials are controlled studies conducted to


evaluate the effectiveness of the drug in a particular indication
and to determine possible side effects and risks. In this phase,
testing determines the safety and efficacy of the drug in
treating the condition and establishes the minimum and
maximum effective dose.

643. Phase III is performed after there is preliminary


evidence that the drug is effective.

644. Phase II is the first phase in which patients with the


target disease or disorder take part.

645. Phase III is the final phase before getting marketing


approval

646. Phase IV trials are post-marketing studies after getting


approval for general sale. They are carried out in order to
gather further information about the drug’s safety, efficacy, and
optimal use.
647. Dogs are more sensitive to drugs than mini-pigs 
648. Choose the incorrect statement about clinical trials:
Clinical trials are mainly aimed at providing medication to
terminal ill patients

649. Participating in clinical trials is a good way to earn some


extra money 

650. The overall benefit-risk of the drug must be evaluated


651. A control group receives either standard medication or
a placebo

652. An inert tablet is called placebo     


653. An adverse event is any abnormal medical occurrence in
a patient or clinical trial subject after a medicinal product has
been administered .

654. In the preclinical stage of drug development, an


investigational drug must be tested extensively in the
laboratory. This is to ensure it will be safe to administer to
humans.

655. The results of all testing must be provided to the FDA in


the United States and/or other appropriate regulatory agencies
in other countries in order to obtain permission to begin
clinical testing in humans.

656. In the preclinical stage of drug development, a(n)


investigational drug must be tested extensively in the
laboratory. This is to ensure it will be safe to administer to
humans.

657. Regulatory agencies require testing that documents the


characteristics - chemical composition,purity quality,and
potency -of thedrug’s active ingredient,and of the formulated
drug.(= strength)
658. Regulatory agencies have to give permission to
commence with the clinical testing in humans.

659. First of all, it is the intention / goal / aim of the


company to complete the preclinical trials by the end of the
year : all of the above

660. Low-dose/mid-dose/high-dose groups are three groups


of animals which receive different concentration (s) of the
medication understudy.

661. A control group in preclinical studies is a group of test


animals that is not exposed to the medication under study. In
an experiment, this group is treated just like the other animals,
but does not receive the active ingredient.

662. The general health and behaviour of the dogs were


checked twice a day.

663. On Day 2, abnormalities regarding food consumption


were observed shortly after administration in the high-
dosegroup.

664. Phase III is performed after there is preliminary


evidence that the drug is effective to obtain additional
information to evaluate the overall benefit-risk relationship of
the drug.

665. Phase II is the first phase in which patients with the


target disease or disorder take part.

666. Phase III Trials: A large group of patients is studied and


closely monitored by physicians for efficacy and any adverse
events after long-term exposure to the drug.

667. Phase IV Trials: They are carried out in order to collect


further information about the drug’s safety, efficacy, and
optimal use.

668. Phase II is performed after there is preliminary


evidence that the drug is effective.
669. The safety and efficacy of a drug can only be determined
by conducting rigorous clinical trials, according to the FDA.(=
very thorough and strict)

670. The parents of a 21-year-old woman challenged the


FDA.They took the authority to court after their daughter had
died of cancer.

671. The safety and efficacy of a drug can only be determined


by conducting rigorous clinical trials, according to the FDA.

Tuầ n 8

672. The Drug Safety department is responsible for: 


Reporting an adverse drug reaction to health authorities /
Responding to a physician’s report about adverse drug
reactions.

673. The Regulatory Affairs department is not responsible


for : Reporting an adverse drug reaction to health authorities /
Responding to a physician’s report about adverse drug
reactions

674. The Regulatory Affairs department is responsible for:


Compiling dossiers for submission to authorities

675. The Drug safety department is not responsible for:


Compiling dossiers for submission to authorities

676. Pharmacovigilance is the practice of monitoring the


effects of medical drugs after they have been licensed for use,
especially in order to identify and evaluate previously
unreported adverse reactions.

677. Pharmacovigilance is the practice where government


agencies, pharmaceutical companies, and healthcare
professionals work together to monitor and evaluate suspected
side effects of medicines to improve the safety of drugs in use.

678. Adverse event is an unwanted medical occurrence


which a patient experiences during treatment. This may or may
not be a side effect of a drug.
679. Side effect is any unintended reaction caused by a drug
or medical treatment. This term is used by the general public,
but is often avoided by medical authorities.

680. A serious adverse event threatens life, requires or


prolongs hospitalization, or results in death.

681. Someone has a(n) rash , that person has a lot of red
spots on the skin.

682. Itching is an uncomfortable sensation in the skin that


feels as if something is crawling on the skin and makes the
person want to scratch the affected area.

683. Irritation means general discomfort, bad feeling.


684. Hypotension is when blood pressure is lower than
normal (e.g. A blood pressure of 80/60).

685. When someone has a blood pressure of 80/60, that


person has Hypotension

686. Heart palpitations is/are the feelings of having rapid,


fluttering or pounding heart, triggered by stress, exercise,
medication or, rarely, a medical condition.

687. Sleeplessness : insomnia


688. A report received from the patient’s sister indicated that
she had history of hypertension.

689. After having taken Mensamint, the patient experience


(ed) headaches and insomnia.

690. A report was received from a physician indicating that a


woman had fainted after developing a sudden, severe skin rash
and inflammation all over her body.

691. The patient reported not having had anything to eat but
a chocolate candy bar 4 hours beforehand.
692. After examining the patient , the attending physician
discontinued Mensamint and administered a strong sedative.

693. After 24 hours, all symptoms had subsided except for a


mild skin irritation and the patient was released from hospital.

694. A correlation between the patient's peanut allergy and


this adserse event cannot be ruled out 

695. The patient's normal vital signs (pulse, blood pressure,


respiratory rate and temperature) were established before the
surgery.

696. The EMEA is a European Union agency for the


evaluation of medicinal products.

697. QPPV is a Qualified Person Responsible for


Pharmacovigilance.

698. Maybe the side effect was a result of taking this


product :  The side effect could have been due to taking this
product

699. old illness : pre-existing conditions 


700. Pharmacopeia is an official publication containing a list
of drugs with their effects and directions for their use.

701. In order to get approval to sell a new drug, a company


has to compile detailed documentation with all the information
required by the drug authorities. Administrative Data
include(s):   general information, such as the marketing
authorization application form, as well as product
characteristics and labelling

702. In order to get approval to sell a new drug, a company


has to compile detailed documentation with all the information
required by the drug authorities. Non-clinical Study Reports
include(s):  study reports, pharmacology, pharmacokinetics,
toxicology, and references
703. PIL : Patient information leaflet
704. Important information for any person taking a drug
found in: Patient information sheet / Patient leaflet / Package
insert    -  All of the above

705. A patient can find Important information about a drug


in: Patient information sheet / Patient information leaflet /
Patient leaflet - All of the above

706. Counterfeit drugs  may contain: a worthless placebo; a


lower concentration of the same active ingredient; a similar,
but different substance; a totally different, potentially
dangerous substance.

707. Fake drugs may contain: a worthless placebo; a lower


concentration of the same active ingredient; a similar, but
different substance; a totally different, potentially dangerous
substance.

708. Choose the incorrect statement about Counterfeit


drugs : Counterfeit drugs are not fake drugs

709. A child may find a pill hard to swallow


710. If symptoms persist, the patient should consult a doctor.
711. This medicine has a bitter aftertaste
712. The patient had a pre-existing condition when he took
the medication.

713. A(n) abdominal pain is the pain in your stomach or


intestines.

714. At the hospital, the patient showed evidence of


hyperactivity , accompanied by confusion and agitation.

715. Government agencies, pharmaceutical companies ,and


healthcare professionals work together to monitor and
evaluate suspected side effects of medicines to improve the
safety of drugs in use

716. Regulatory Affairs department is responsible for


compiling dossiers for submission to authorities, submitting
documents needed to obtain marketing approval for a drug,
and writing the drug information for the patient.

717. Ms Gallois, the well-known opera singer, lost


consciousness 30 minutes before she had planned to go on
stage. ( = the condition of being awake and able to understand
what is happening around you)

718. contraceptive is a drug or method used to prevent a


woman from becoming pregnant when she has sex.

719. Serious adverse event (SAE) - an adverse event that


threatens life, requires or prolongs hospitalization, or results in
death.

720. The patient's normal Vital signs (pulse, blood pressure,


respiratory rate and temperature) are established in the pre-
operative period and variations 10% above or below the pre-
operative measurement should be reported immediately.

721. If you feel dizzy , you feel that you are losing your
balance and are about to fall.

722. If you faint, you lose consciousness for a short time,


especially because you are hungry, or because of pain, heat, or
shock.

723. Do not take Mensamint TM if you are allergic to


penicillin.

724. The patient has an allergy to peanuts


725. The evidence is inconclusive.The facts neither prove nor
disprove this.
726. In order to get approval to sell a new drug, a company
has to compile detailed documentation with all the information
required by the drug authorities

727. We do need to let patients know of any possible side


effects. But, it is not necessary to alarm them unnecessarily.

728. When describing possible side effects for products in


the pipeline, we will need to differentiate more clearly between
common and rare risks.

729. A high-profile person or a high-profile event attracts a


lot of attention or publicity. (= famous)

730. Our patients shouldn’t be so alarmed that they are


afraid to actually put the pills in their 

731. It has the same packaging, same colour coating, same


bitter aftertaste, but not the same ingredients inside the pill. Is
this a fake drug?

732. In Europe, steps have been taken to use holograms to


prove a pharmacopeias authenticity.

733. Excipient is an inactive substance that serves as the


vehicle or medium for a drug or other active substance.

734. A(n) fatal accident or illness causes someone's death.


Tuầ n 9
735. A four year old boy was found dead after he had stuck a
highly potent, pain relieving patch to his leg.

736. A jar is a multi-use glass container with a twist-on lid. It


can hold pharmaceuticals, or any kind of fluids or solids. It can
be opened and closed several times until the contents are used
up. Sometimes a desiccant is integrated into the cap so that the
contents remain dry.
737. A sachet is a small disposable bag containing an
individual dose of the medicine. It often has a lengthwise
perforation which can be torn open.

738. The wet granules are pressed through a Sieve on their


way to the fluid bed dryer.

739. The dried granules are stamped into a mould to form


tablets.

740. A jar is a multi-use glass container with a twist-on lid. It


can hold pharmaceuticals, or any kind of fluids or solids. It can
be opened and closed several times until the conten (s) are
used up. Sometimes a desiccant is integrated into the cap so
that the conten (s) remain dry.

741. The moisture is removed by the hot air in the fluid bed
dryer.

742. A first layer must be peeled off a blister before the drug
can be pushed through the second layer: peel-push system
(Container system

743. A  drum holds the pressed tablets until it is time to coat


them.

744. effervescent tablets are uncoated tablets containing


substances that react in the presence of water and give off
carbon dioxide.

745. A(n) sachet is a small disposable bag containing an


individual dose of the medicine. It often has a lengthwise
perforation which can be torn open.

746. If someone is convict (d) of a crime, they are found


guilty of that crime in a law court.

747. Well, we have to make sure that there are no mix-up (s)
(mistake) of materials throughout the whole manufacturing
process.
748. Safety goggles are used to protect your eyes are you
work in the lab such as chemical splashes/spills.

749. Primary packaging is the material which is in direct


contact with the product.

750. During the manufacturing process, technicians also


check the samples for content uniformity, content weight, and
so on.

751. A(n) jar is a multi-use glass container with a twist-on


lid. It can hold pharmaceuticals, or any kind of fluids or solids.
It can be opened and closed several times until the contents are
used up. Sometimes a desiccant is integrated into the cap so
that the contents remain dry.

752. In the Excess powder remover, As the tablets go up a


spiral, they are shaken, and the excess powder is vacuumed off.
The pressed tablets are put into a drum and stored until it is
time to coat them.

753. A jar is a multi-use glass container with a twist-on lid. It


can hold pharmaceuticals, or any kind of fluids or solids. It can
be opened and closed several times until the contents are used
up. Sometimes a desiccant is integrated into the cap so that the
contents remain dry.

754. Lab equipment should always be clean or sterile and


calibrate (d) before using it.

755. The granules are air-dried in the Fluid bed dryer.


756. dispenser is a machine/ mechanism which releases its
contents in defined amounts.

757. Safety is the freedom from danger or harm.


758. A tube that can only be released by an adult-length
finger by pushing an internal catch.

759. humidity is the amount of water vapor in the air


760. A(n) blister pack is a type of single-use plastic container,
and is used for pharmaceutical products as well as for other
consumer goods. The product is placed in the formed cavity
and sealed by lidding foil. The product is removed by pushing it
through the foil.

761. In a "push-screw" container system, a closure must be


pushed down before it can be unscrewed.

762. A few years ago, a mother was convicted of negligence


leading to her son's death. It was claimed that he had died from
a pain medication overdose.

763. The dried granule s) are stamped into a mould to form


tablets.

764. rubber gloves protect hands from chemical compounds


765. If you give instructions in a very direct way, it may not
sound polite.

766. Slide container system is a container with three buttons


that must be align ed) in order to slide off the lid .

767. A sachet is a small disposable bag containing a(n)


individual dose of the medicine. It often has a lengthwise
perforation which can be torn open.

768. A drum holds the pressed tablets until it is time to coat


them

769. A blister pack is a type of single-use plastic container,


and is used for pharmaceutical products as well as for other
consumer goods. The product is placed in the formed cavity
and sealed by lidding foil. The product is removed by pushing it
through the foil

770. The boy's death highlighted a problem that no one had


anticipate (d) up to that time .
771. lab coat protects the scientist and the scientist's clothes
from hazardous or hot chemicals

772. A(n) Inhaler is an aerosol dispensing device which


releases medication into the mouth of the patient. The
medication is breathed deeply into the lungs, or stays in the
mouth or throat.

773. Pharmaceutical companies have to comply with GMP


guidelines

774. During the manufacturing process, technicians also


check the samples for content uniformity, content weight, and
so on.

775. Please mind the corrosive substances, which could


cause severe burns.

776. Which primary packaging is the most suitable for


ointments?  Tube 

777. In order to receive valid and reliable results, all devices


and methods have to undergo a validation process.

778. Which primary packaging is the most suitable for nose


drops?  bottle

779. A vacuum system sucks up the excess powder.


780. Secondary packaging is any packaging material that is
not in direct contact With the product.

781. premises is a place where company has its offices and/


or factories.

782. A shaker loosens the excess powder.


783. A few years ago, a mother was convicted of negligence
leading to her son's death. ( = Failure to take proper care over
something/someone)
784. A lot of research is done to make packaging
childproof,i.e. a child cannot open it alone. However, at the
same time, the elderly must have easy access to their
medication,i.e.it needs to be elderly- accessible.

785. A container with three buttons that must be aligned in


order to slide off the lid.  slide (Container system)

786. A hard hat must be worn at all times in this area to


protect your head.

787. A(n) sticky label is a piece of paper attached with


adhesive to the primary packaging to identify it and give details
concerning its ownership, nature, and/or use.

788. GMP covers how to design and construct buildings so


that the flow of materials is optimize (ed), and so that they can
be cleaned easily.

789. Dry ingredients are weighed and transported to the


granulator by the Hoist.

790. childproof means a child cannot open it alone.


791. A tube that can only be released by an adult-length
finger by pushing an internal catch.  poke (Container system)

792. The dried granules are stamped into a mould to form


tablets in the Tablet press.

793. Nowadays, RRB is a research-driven,innovative


pharmaceutical enterprise that develops new drugs, produces
them, prepares them for sale, and markets them worldwide.

794. Security  is the protection from threats, such as attacks


or crime.

795. In the Granulator,  the ingredients are mixed to create a


wet mixture.
796. A mother was sentenced to several years' community
service for leaving a used medical patch in a place where her
young son could have access to it.

797. A closure must be pushed down before it can be


unscrewed : push-screw (Container system)

798. The elderly must have easy access to their


medication,i.e.it needs to be elderly-accessible.

799. Safe-disposal boxes should be included in the packages


of medicated patches. These boxes should have a small slit at
the top to discard used patches and it should be impossible to
open them.

800. A closure must be squeezed between two fingers before


it can be unscrewed : squeeze-screw (Container system)

801. Because of her son's death, the young mother demand


(ed) that safe-disposal boxes be included in the packages of
medicated patches.

802. Pharmaceutical companies have to comply with GMP


guidelines.

803. A(n) syringe is a needle attached to a plastic tube used


for putting medicine into the body or removing blood.

804. In the meantime, requirements have reached a very


high standard.

805. When it was founded, the company only had one


production site.

806. During the safety film, I will give you more detailed
information on the company.

807. Once  the tour is finished, you will have seen the most
important production areas.
808. The clothing specifications didn’t use to be
documented. 

809. The company’s safety regulations didn’t use to be so


strict.      

810. The company’s safety regulations didn’t use to be so


strict.

811. Dry ingredients are weighed and transported to the


granulator by the hoist.

812. In the granulator, the ingredients are mixed to create a


wet mixture.

813. The granules are air-dried in the fluid bed dryer. 


814. The excess powder is loosened by a shaker
815. In the tablet press, the dried granules are stamped into
a mould to form tablets.

816. Primary packaging is the material which is in direct


contact with the product.

817. Secondary packaging is the material which is not in


direct contact with the product.

818. A(n) sachet is a small disposable bag containing an


individual dose of the medicine. It often has a lengthwise
perforation which can be torn open.

819. A(n) inhaler is an aerosol dispensing device which


releases medication into the mouth of the patient. The
medication is breathed deeply into the lungs, or stays in the
mouth or throat.

820. A(n) syringe is a needle attached to a plastic tube used


for putting medicine into the body or removing blood.
821. A(n) sticky lable is a piece of paper attached with
adhesive to the primary packaging to identify it and give details
concerning its ownership, nature, and/or use.

822. A jar is a multi-use glass container with a twist-on lid. It


can hold pharmaceuticals, or any kind of fluids or solids. It can
be opened and closed several times until the contents are used
up. Sometimes a desiccant is integrated into the cap so that the
contents remain dry

823. A sachet is a small disposable bag containing an


individual dose of the medicine. It often has a lengthwise
perforation which can be torn open.

824. What type of packaging material is a syringe ? Primary 


825. What type of packaging material is a sachet ?  Primary
826. Which primary packaging would you recommend for
nose drops ?  bottle

827. Which primary packaging would you recommend for


ointments ?  tube

828. Which primary packaging would you recommend for


oral tablets ?  blister pack

829. Which primary packaging would you recommend for


eye drops?  bottle

830. To use a blister pack, you push through it. 


831. A patient needs to press an inhaler to use it. 
832. Choose the CORRECT matching of packaging material
and the verb used to describe how to use them:  a jar - twist

833. A lot of research is done to make packaging


childproof ,i.e. a child cannot open it alone.
834. In a push-screw container system, a closure must be
pushed down before it can be unscrewed.                    

835. In a peel-push container system, a first layer must be


peeled off a blister before the drug can be pushed through the
second layer

836. In a slide container system, a container with three


buttons that must be aligned in order to slide off the lid.

837. security  : Protection from threats, such as attacks or


crime

838. Our documentation must be improved to meet  the


requirements of the regulatory authorities.

839. If a pill has a brightly-coloured coating a child may


mistake it for a sweet.

840. Uncomplicated :  simple


841. Nowadays, RRB is a research-driven, innovative
pharmaceutical enterprise that develops new drugs, produces
them, prepares them for sale, and markets them worldwide.

842. effervescent tablets are uncoated tablets containing


substances that react in the presence of water and give off
carbon dioxide.

843. A hard hat must be worn at all times in this area to


protect your head.

844. Safety is the freedom from danger or harm 


845. If you give instructions in a very direct way, it may not
polite.

846. The moisture is removed by the hot air in the fluid bed 
847. A jar is a multi-use glass container with a twist-on lid.
Sometimes a(n) desiccant is integrated into the cap so that the
contents remain dry.

848. huminity is the amount of water vapor in the air 


849. A sachet is a small disposable bag containing an
individual dose of the medicine. It often has a lengthwise
perforation which can be torn open.

850. child proof means a child cannot open it alone. 


851. Because of her son's death, the young mother demand
(ed) that safe-disposal boxes be included in the packages of
medicated patches.

852. Safe-disposal boxes should be included in the packages


of medicated patches. These boxes should have a small slit at
the top to discard used patches and it should be impossible to
open them.

You might also like