Jurisprudence Pharmacy Quiz-I | GPAT, DI, B.Pharm, D.Pharm & M.Pharm

Answer key:- at the end of the page

1. List of the substances that are required to be used only under medical supervision and which are labeled accordingly is/are

1. R
2. {c}G
3. P
4. C and C₁

2.Establishment(s) which has/have a qualified person engaged in compounding of drug is/are

1. Drug store
2. Chemist and druggist
3. {c}Pharmacy
4. None of these

3. License for wholesale of drugs specified in the schedule C and C₁ is issued in Form

1. 20-A
2. 20-B
3. {c}21-B
4. 22-A

4. The left-hand top corner of the label of schedule X bulk drugs contains symbols,

1. R_X
2. RMP
3. X
4. {c}XR_X

5. In the constitution of state Pharmacy Councils, total number of Registered Pharmacists to be elected is

1. Five
2. {c}six
3. seven
4. four

6. The Drugs and cosmetics Rules were passed in the year of

1. {c}1945
2. 1947
3. 1944
4. 1946

7. How many representatives are nominated by the central government to Drug Consultative committee?

1. 1
2. {c}2
3. 3
4. 4

8. The sample taken by the Drug Inspector from the retail premises should be divided into

1. {c}4 parts
2. 3 parts
3. 2 parts
4. 5 parts

9. As per GMP, during tablet compression, in process control should be done at regular intervals of

1. Not more than 45 minutes
2. Not more than one hour
3. Not more than 30 minutes
4. Every one hour

10. Equipment recommended for the manufacture of powders come under

1. Schedule H
2. {c}Schedule M
3. Schedule N
4. Schedule X

11. Magic remedies include

1. Talismans    
2. Mantras
3. Kavachas
4. {c}All of these

12. Spurious drugs means

1. imitations
2. Substitutes
3. Resembling othr drugs
4. {c}All of these

13. GMP for Ayurvedic, Siddha and Unani medicines are covered by

1. Schedule U
2. {c}Schedule T
3. Schedule W
4. Schedule M

14. Quality control of vaccines is carried out by ……………. Studies

1. In vivo
2. In vitro
3. {c}In vivo and in vitro
4. Neither in vivo nor in vitro

15. Drugs Technical Advisory Board (DTAB) – Allopathy consists of 18 members whereas DTAB- Ayurvedic, Siddha and Unani drugs consists of

1. 18 members
2. 20 members
3. 15 members
4. {c}None of these

16. The list of disease for which advertisement banned or prohibited is finalized in consultation with

1. {c}Drugs Technical Advisory Board
2. Drugs Testing Laboratory
3. Central Drugs Laboratory
4. None of these

17. Which one of the following is not the wing of Drugs and Cosmetics Act?

1. Advisory wing
2. Analytical wing
3. Administrative wing
4. {c}Education and pharmacy wing

18. Schedule M incorporating GMP (Good manufacturing practices) was introduced in

1. 1987
2. {c}1988
3. 1989
4. 1990

19. The first schedule of drugs and cosmetics act, 1940 comprises

1. {c}The list of books of references for Ayurvedic, Siddha and Unani medicines
2. List of pharmacy books
3. List of Homeopathic books
4. None of these

20. The committee appointed by Government of India to look into the drug industry and various aspects of drugs like licensing, price control, imports, role of foreign sector, quality control was headed by

1. Mudaliar
2. Bhatia
3. {c}Hathi
4. Bhore

21. The poison act was introduced in the year

1. 1878
2. 1894
3. {c}1919
4. 1930

22. Fine for false claim to be a registered pharmacist on first conviction is

1. {c}Rs. 500
2. 6 months imprisonment
3. Rs. 1,000
4. Both fine and imprisonment

Answer Key

Q. No	Ans	Q. No.	Ans
1	2	12	4
2	3	13	2
3	3	14	3
4	4	15	4
5	2	16	1
6	1	17	4
7	2	18	2
8	1	19	1
9		20	3
10	2	21	3
11	4	22	1

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