COURSE- B.

Pharmacy Semester/Year -
Subject Name : Pharmaceutical Jurisprudence SUBJECT CODE-
Sr.No. Unit No. Question
1 3 As per Drugs and Cosmetic Act,’ standard drug’ is one
2 3 Analysis and test of samples of vaccines are carried out at
3 3 As per Schedule M, the permi ed limit of solid content inwater for injec on is…..

4 3 A person is called as “Registered Pharmacist”, if he is

5 3 Standard of Quality for drugs are prescribed in
6 3 Cosmetics means any article intended to
7 3 Biological and microbiological tests are carried out at….
8 3 A non bonded manufactory shall inspected by the otherofficer at least
9 3 Whole human blood can be stored for…
10 3 Applica on to manufacture cosme cs is made to thelicensing authority in….
11 3 Requirements of factory premises for manufacture ofmedical devices id dealt under
12 3 Under Sec on 21 of the Indian penal code, all DrugInspectors are…
13 3 The label of any Homeopathic Medicine should bear thepotency of the medicine in…..
14 3 Any person who has been convicted of criminal conspiracyto commit any of the offences listed und
15 3 The PCI was first constituted on….
16 3 For the registra on of pharmacist in the various states, thePharmacy Act provides liar the cons tu
17 3 The manufacture and sale of cosme cs licensed as toothpastes containing…..have been prohibited
18 3 Different Forms for application to procure licence, renewal of licence, and for all other activities.
19 3 Rates of fees charged for analysis by COL or State Drugs Laboratories.
20 3 List of biological and other special products governed by special provisions
21 3 Class of drugs: extent and conditions of exemption
22 3 List of poisonous substance under Ayurvedic , Siddha and Unani medicines
23 3 Standards for Umbilical tapes
24 3 Standards for ophthalmic preparations
25 3 Drugs required to be taken under medical supervision.
26 3 List of prescription drugs
27 3 List of diseases or ailments which a drug may not purport to prevent or cure.
28 3 Drugs exempted from certain provisions related to manufacturer
29 3 GMP (Good Manufacturing Practices) comprising requirements of factory premises, plant and equi
30 3 Cosmetics - requirements of factory premises for manufacture
31 3 Requirements of factory premises for manufacture of medical devices
32 3 List of minimum equipment of running a pharmacy
33 3 Standards for disinfectant fluids
34 3 Life period of drugs
35 3 Pack sizes of drugs
36 3 List of colours, dyes and pigments permitted in cosmetics and soaps, list of colours permitted in so
37 3 Standards for condoms of rubber latex and other mechanical contraceptives
38 3 Standards for medical devices
39 3 Standards for Cosmetics
40 3 GMP (Good Manufacturing Practices) for manufacture of Ayurvedic, Siddha and Unani medicines, G
41 3 Particulars required to be shown in manufacturing records; raw material and analytical records
42 3 Particulars required to be shown in manufacturing records.
43 3 Standards for patent or proprietary medicines
44 3 Psychotropic substances
45 3 Requirements and guidelines on clinical trials for import and manufacture of new drug
46 3 cold place
47 3 Cool place
48 3 Room temperature
49 3 Freezer
50 3 Qualification for Drug Inspector
Semester/Year -

ANSWER Option-A Option-B Option-C

That Complies with the standard of Drug
That Compiles
and Cosme with
c standards
That Compiles
of official
with
pharmacopoeia
That
international
Compilesstandards
with the standard of na onal an
Central Research Institute, Kaushali Central Indian Pharmacopeia
PasteurLaboratory,
Institute ofGhaziabad
Central
India, Coonoor
Drug Testing Laboratories, Thane
10 ppm 10 ppm 100 ppm 0.1 ppm

Having his name entered in the stateHolding

registerdiploma
of in pharmacy
Having sufficient experience
Having hisinname
pharmacy
entered
profession
in the state register of
The Second Schedule to the D& C act,1940
The first schedule to D&CTheAct,1940
Second Schedule The
to Schedule
the D& C Dact,1940
to the Drugs and Cosmetic Rule
Alter the appearance of the human body
Affect the structure of the
Destruct
humanvermin
body of insects
Alter the appearance of the human body
Central Research Institute, Kasauli Central Research Institute,
National
Kasauli
Institute ofCentral
Biologicals,
DrugsNoida
Research Institute, Lucknow
Once every month Once every month Once every two months Once every six months
21 Days 12 Days 24 Days 21 Days
Form 31 Form 31 Form 31A Form 32
Schedule M3 Schedule M1 Schedule M2 Schedule M3
Public Servants Qualified persons Competent PersonsPublic Servants
Decimal Decimal Milligram gram
Death penalty Life Imprisonment Death penalty Solitary confinement
9 th March,1949 6 th March,1950 9 th March,1949 9th May,1940
Registrar of State pharmacy council Registration Tribunal Co-operative SocietyRegistrar of State pharmacy council
Tobacco Fluoride content more than
Calcium
1000
carbonate
ppm more
Tobacco
than 1000 ppm
Schedule A Schedule A Schedule B Schedule C
Schedule B Schedule A Schedule B Schedule C
Schedule C Schedule A Schedule B Schedule C
Schedule D Schedule A Schedule B Schedule C
Schedule E Schedule FF Schedule E Schedule F
Schedule F (III) Schedule F (II) Schedule F (III) Schedule F
Schedule FF Schedule FF Schedule F (III) Schedule F
Schedule G Schedule FF Schedule F (III) Schedule F
Schedule H Schedule B Schedule H Schedule F
Schedule J Schedule J Schedule H Schedule F
Schedule K Schedule J Schedule K Schedule F
Schedule M Schedule M Schedule K Schedule F
Schedules M-(II): Schedule M Schedules M-(II): Schedule D
Schedules M-(III): Schedule M Schedules M-(III): Schedules M-(II):
Schedule N Schedule M Schedules M-(III): Schedule N
Schedule O Schedule O Schedule N Schedule K
Schedule P Schedule P Schedule N Schedule K
Schedule P-l Schedule P Schedule P-l Schedule K
Schedule Q Schedule O Schedule P Schedule K
Schedule R Schedule R Schedule P Schedule K
Schedule R-I Schedule R Schedule R-I Schedule K
Schedules S Schedules S Schedule R- Schedule K
Schedules T Schedules S Schedules T Schedule K
Schedules U Schedules S Schedules T Schedule K
Schedules U (1 Schedules U (1 Schedules T Schedule K
Schedules V Schedules U (2 Schedules V Schedule K
Schedules X Schedule P Schedules V Schedule K
Schedules Y Schedules Y Schedules V Schedule K
2-8° C 2-10° C 2-8° C 5-10° C
8° C and 25° 2-10° C 2-8° C 5-10° C
the temperature prevailing in a working
2-10°area
C the temperature prevailing
5-10° C in a working area
between −20° C and −10° C between −20° C and −10° theCtemperature prevailing
5-10° C in a working area
(i) a drug inspector with atleast 18 months
(ii) a drug
of experience
inspector with
inamanufacturing
drug
atleast
inspector
3 yearsofwith
experience
atleast
(i)minimum
a drug
oneininspector
substance
inspecting
of 18 months
with
specified
theatleast
firms
experience
inmanufacturing
18
Schedules
months
in testing
of
C an
e
Option-D
That Complies with the standard of Drug and Cosme cAct
Central Research Institute, Kaushali
1 ppm

Holding degree in pharmacy

The schedule J to the D&C Rules,1945
All of the above
Central Drugs Laboratory, Kolkata
Once every ten year
64 Days
Form 32A
Schedule R1
Officer-in-charge, Drug Control
Parts per Mole
Corporal punishment
6th May,1940
Registrar of central pharmacy council
Menthol more than 0.12%
Schedule D
Schedule D
Schedule D
Schedule D
Schedule D
Schedule G
Schedule G
Schedule G
Schedule G
Schedule G
Schedule B
Schedule B
Schedule B
Schedule K
Schedule K
Schedule G
Schedule G
Schedule G
Schedule Q
Schedule Q
Schedule Q
Schedule Q
Schedule Q
Schedules U
Schedule Q
Schedule Q
Schedules X
Schedules X
5-20° C
5-20° C
5-20° C
5-20° C
All of the above