VIETNAM UNIVERSITY OF TRADITIONAL MEDICINE

DEPARTMENT OF FOREIGN LANGUAGES – ENGLISH GROUP

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SAMPLE TEST 1
Goods: hàng hóa, sản phẩm, make sure= ensure that + Mệnh đề
I. Choose the best answer A, B, C or D to complete the following sentences. (15)
1. The practice of making sure that …………… and services fulfil defined standards
is called the ……………
A. goods/ quality assurance: QA B. substances/ compliance
C. substances/ prescription: sự kê đơn>< non- prescription= OTC (over-the-
counter) D. goods/ GMP : Good Manufacturing Practice
2. In order to get approval to sell a new drug, a company has to compile detailed
documentation with all the information required by the ……………. Compile: tổng
hợp
A. regulatory affairs B. SOPs: Standard Operating
Procedures
C. drug authorities D. QA: Quality Assurance
3. Some of the work the lab technicians do for the production department includes
various ……………. during the process contamination= pollution: bẩn, ô nhiễm><
pure, purity
A. interim analyses B. safety protections
C. active material creations D. contamination tests
4. In the PIL, basically for side effects that are ……………., you don’t just use “this
lead to”. Instead, say “this may, might, or can lead to”. However, in the case of
……………. side effects and real warning, it is really necessary to be direct.
A. not common/ common B. common/ not common pill:
viên tròn, PIL: Patient Information Leaflet: Giấy hướng dẫn sử dụng thuốc cho
bệnh nhân
C. not common/ rare D. unwanted/ real
5. …………… in clinical trials is a good way to …………… some extra money
ToV: Đứng làm chủ ngữ: mang nghĩa ở TH sử dụng ẩn ý, participate in= take
part in
A. To participate / earn B. Participating/ spend
C. To participate/ spend D. Participating/ earn earn money:
kiếm tiền
6. …………… to humans are determined in toxicity studies.
A. Extensive documentation B. Clinical trial
C. Intended drugs D. Potential risks
7. Phase I Trials are done to find out how the drug …………… in the body. Drug
….body
A. works B. respond C. reacts D. all of the
above
8. In the preclinical stage of drug development, an investigational drug ………….
extensively in the laboratory. Must be +V pii
A. would be B. must be tested C. have to be tested D. ought to
9. The active ingredient can be tested in humans only after preclinical tests have
been successfully completed and …………… has been given.
 A. documentation B. permission C. information D. authorization
10. Some of her symptoms are known …………… of Mensamint: loss of sleep if
taken in the late afternoon or evening, increase in blood pressure, heart
palpitations, and headaches.
A. unwanted occurrence B. side effects
C. intended reactions D. All are correct
11. We need to remember that not only healthcare ……………. read these PILs, but
also ……………. Healthcare professional: chuyên gia chăm sóc sức khỏe, PILs:
Patient Information Leaflets:
A. pharmacists/professionals B. patients/ patient’s family
C. professionals/ patients D. doctors/ technicians
12. When using Pogolox , tell your doctor right away if your ……………. continues
TM

to rise. Right away= immediately: ngay lập tức, rise không đi kèm với tân ngữ
Raise: Raise your hand: Raise+ tân ngữ
A. pulse: mạch B. breath C. temperature D. high
blood pressure
13. Please remember that the overshoes are only allowed to touch the …………….
A. white area B. black area C. color area D. All are
correct
14. Regulatory agencies require testing that …………… the characteristics and
chemical composition of the API and …………… drug API: Active Pharma
Ingredient: Thành phần hoạt chất
A. document / formulation B. documents / formulated

C. writes / formed D. note down / formulary

15. A(n) ……………. is a piece of paper attached with adhesive to the …………….
to identify it and give details concerning its ownership, nature, and/or use
A. sticky label / primary packaging B. syringe/ secondary packaging
C. sachet/ primary packaging D. blister pack/ secondary packaging
Sachet: gói, blister pack: vỉ
II. Read the sentence and decide if it is True (T) or False (F) by choosing the
answer A or B. (5)
1. All laboratory work must be documented in accordance with GLP. Good
Laboratory Practice:
A. T B. F in compliance with
2. According to the names of health authorities and terms used in pharmacovigilance,
EMEA stands for European Medicines Agency.
A. T B. F
3. It is absolutely essential to move lab mice outdoors in closing cages closed
A. T B. F
4. The quality assurance process in good manufacturing practice includes product
quality control, enables traceability, and testing. sampling
A. T B. F
5. In preclinical trials, there are at least two different animal models. They are
rodents and animals which have systems more similar to human.
A. T B. F
III. Read the text and choose the answer A, B, C or D to fill in the blanks with
missing information.
Primary=main=necessary=compulsory neither…nor, either…or
The primary job responsibilities of Pharmacovigilance professionals are to provide
product/drug safety data and documentation. Pharmacovigilance professionals are
qualified drug safety specialists.  One particular area of their work includes
performing a lot of functional responsibilities like safety trend analysis,
maintaining adverse reaction data, keeping global safety databases updated and
conducting safety training.

Pharmacovigilance is a pharmacological science that helps us to better evaluate the

undesired effects of drugs, report “them” to the applicable authorities and thus help
in ensuring that only safe drugs stay in the market. For that reason “it” is an extremely
important job function. Pharmacovigilance professionals gather adverse drug reactions
and safety data from people who have experienced an adverse effect, healthcare
providers like physicians as well as hospitals.

1. Providing product/drug safety data and documentation are ……………. of

Pharmacovigilance professionals.
A. main essential functions (A) B. job responsibilities (B)
C. Neither A nor B is correct D. Both A and B are correct

2. Pharmacovigilance professionals are …………….

A. drug safety specialists B. qualified drug safety
specialists
C. qualified specialists D. specialists
3. There are ……………. examples of functional responsibilities performed by
Pharmacovigilance professionals.
A. two B. three C. four D. five
4. The word “them” in paragraph 2 refers to …………….
A. pharmacovigilance B. pharmacological science
C. the undesired effects of drugs D. the applicable authorities
5. The word “it” in paragraph 2 refers to …………….
A. pharmacovigilance (A) B. pharmacological science (B)
C. Neither A nor B is correct D. Both A and B are correct

IV. Read the text below and choose ONE suitable word from the given ones to fill
in each numbered blank. Significant=important: quan trọng, living organisms:
sinh vật sống

organisms rats Relationship used humans

toxicology scientific Means refers substances
The dose of the substance is an important factor in toxicology, as it has a significant
(1) ……relationship ………… with the effects experienced by the individual. It is
the primary (2) ……means ………… of classifying the toxicity of the chemical, as it
measures the quantity of the chemical, or the exposure to the substance. All (3) …
substances… ………… have the potential to be toxic if given to living (4) …… …
organisms……… in the right conditions and dose.
LD50 is a common term used in (5) ……toxicology ………… , which (6) …… …
refers……… to the dose of a substance that displays toxicity in that it kills 50% of a
test population. In (7) … …scientific………… research, (8) ……rats… ……… or
other surrogates are usually (9) ………used ……… to determine toxicity and the data
are extrapolated to use by (10) …… humans…………. (119 words)