PHARMACEUTICAL JURISPRUDENCE QUESTION BANK (B-PHARM V-SEM)

LONG QUESTIONS (10 MARKS)

1. Write in brief about whole sale and retail sale.
2. Explain the conditions to grant license for manufacture of drugs specified in schedule C, C1 and X.
3. Explain the conditions to grant license for manufacture of drugs specified other than schedule H &
X.
4. What are the precedents and subsequent conditions for grant of license to manufacture of drugs
and cosmetics specified in schedule C, C1 and X?
5. Write the conditions to grant license for manufacture
a) Drugs for purpose of examination, test and analysis.
b) Loan licenses
6. Explain in detail about manufacture of new drug, loan license and repacking license.
7. Explain the various licenses issued under Drug and Cosmetics Act 1940.
8. Describe the classes of drugs and cosmetics which are prohibited from import and import under
License.
9. Explain in detail about schedule M.
10. Discuss the penalties for manufacturing and sale of drugs in contravention of Drugs and Cosmetics
Act 1940.
11. Explain in detail about prohibition of manufacture and sale of certain drugs under Drugs and
Cosmetics Act 1940.
12. Explain briefly about schedule Y.
13. Explain in detail about schedule M.
14. Discuss briefly about clinical trials as per schedule Y.
15. Write the constitution and functions of Drug Technical Advisory Board
16. Write the constitution and functions of PCI.
17. Explain in detail about Education Regulation (ER) 1991.
18. Write in detail about Education Regulation of State and Joint State Pharmacy Councils.
19. Define Education Regulation. Mention the standards, regulations prescribed for Education
Regulation.
20. What are subsequent registers? Mention the qualifications required for entry into first and
subsequent registers.
21. Give the design of bonded laboratory. Discuss in detail about manufacturing of alcoholic
preparations in bonded laboratory.
22. Give the design of non-bonded laboratory. Discuss in detail about manufacturing of alcoholic
preparations under non-bonded laboratory.
23. Define Drug Inspector. Mention the qualifications, degrees and powers of Drug
24. Write the objectives of NDPS Act 1985. Discuss briefly about offences and penalties of NDPS
Act 1985.
25. Give a detailed account on cultivation, production and sale of poppy straw.
26. Define code of ethics. Explain receiving and handling of prescription of pharmacist.
27. Give the constitution and functions of Institutional Animal Ethical Committee (IAEC).
28. Write the objectives and prevention of cruelty to animals. What are the parts of CPCSEA
guidelines?
29. What are CPCSEA guidelines for breeding and stocking of animals?
30. Write about transport and acquisition of animals for experiment.
31. Write a note on power to suspend or revoke of registration as per Prevention of Cruelty to
animals Act.
32. Describe the facilities to be maintained for experimentation on animals under CPCSEA
guidelines.
33. Write salient features of drugs and magic remedies act and its rules.
34. Write a note on transfer and acquisition of animals for experiments.
35. Write a note on sales price of bulk drugs.
36. Describe the procedure for obtaining a patent? Write a note on opposition to grant of patents?
37. Write constitution of central information commissions.
38. Write in detail about pharmaceutical legislation.
39. Describe the ethics for pharmacist in relation to his job during his service.
40. Describe the ethics for pharmacist in relation to his trade.
41. Describe the ethics for pharmacist in relation to his medical profession.
42. Write a detail note on IPR?
43. Write a pharmacist Oath?
SHORT QUESTIONS (2 MARKS)

1. Give offences and penalties about import of drugs.

2. Write about import of drugs for personal use.
3. Write about import of new drugs.
4. Give two examples of permitted colors as per Drugs and Cosmetics Act 1940.
5. Write places from which drugs are imported in India.
6. Define drugs and cosmetics as per Drugs and Cosmetics Act
7. Write about manufacturing of new drugs.
8. Define spurious drugs as under Drugs and Cosmetics Act.
9. Define misbranded and adulterated drugs.
10. Mention the rules for drugs and cosmetics.
11. Define Patent or Proprietary medicine.
12. Define Government Analyst.
13. Define loan license.
14. Write any two offences and penalties for sale of drugs.
15. Enumerate two functions of PCI Inspector.
16. Give the labelling requirements and write specimen label for schedule G.
17. What is Drug Consultative Committee (DCC)?
18. Write a note on repacking license.
19. Enumerate schedule B.
20. Write the types of retail sale of drugs. Give two examples of schedule J.
21. Write a short note on Drug Control Laboratory.
22. What is schedule G & N.?
23. Write the labelling requirements for ophthalmic preparation.
24. Write about preparation of first register.
25. Mention the offences and penalties in contravention of Pharmacy Act.
26. Differentiate between State and Joint State Pharmacy Council.
27. Define Education Regulation.
28. Mention the ex-officio members of PCI.
29. Define London proof spirit under M&TP Act.
30. Define rectified spirit as per M&TP Act.
31. Write a short note on Central Drugs Standard Control Organization (CDSCO).
32. What is the punishment specified for illegal cultivation of coca plants?
33. What are objectives of NDPS Act?
34. Define cannabis under NDPS Act. 4. State clandestine arrangement.
35. Write a short note on National List of Essential Medicines (NLEM).
36. Explain Drugs Price Control Order (DPCO).
37. Write a note on retail price and ceiling price of scheduled formulations.
38. Write a short on sale price of bulk drugs and retail price of formulations.
39. Who maximum allowable post manufacturing expenses (MAPE) is calculated as per DPCO.
40. Write about CPCSEA.
41. Define contact research & Collaborative research
42. Write a note on National list of essential medicine.
43. Define market share.
44. What is prohibited advertisement.
45. Give two recommendations made by Bhatia committee.
46. Give the significance of Drugs Enquiry Committee (DEC).
47. Give any three recommendations of Hathi committee.
48. Write about Mudaliar committee.
49. What is Chopra’s committee?
50. Mention the objectives of Pharmaceutical Legislations.
51. What is Hathi committee?
52. Write a note on health survey of Pharmaceutical Legislation.
53. Define Pharmaceutical Legislation.
54. Write a brief review on Pharmaceutical Legislation.
55. What is Apprentice Pharmacist as per the code of pharmaceutical ethics?
56. Enlist the code of pharmaceutical ethics in relation to medical profession.
57. How a pharmacist should follow fair trade practice as per code of pharmaceutical ethics.
58. Describe professional vigilance as code of pharmaceutical ethics.
59. Define Pharmaceutical Ethics.
60. Reproduce pharmacist’s oath.
61. Write a brief note on code of pharmaceutical ethics.
62. Differentiate between ethics and laws.
63. Write the role of pharmacist in health care system.
64. Write a short note on termination of pregnancy as per MTP Act.
65. Describe the places where pregnancy may be terminated as per MTP Act.
66. Write a short note on role of Chief Medical Officer (CMO).
67. Mention the objectives of MTP Act.
68. Mention the circumstances under which pregnancy can be terminated.
69. Mention the offences and penalties of MTP.
70. Write a note on Central Information Commission.
71. Write a note on State Information Commission.
72. Define Right to Information.
73. What are the duties of Right to Information?
74. Enumerate the functions of Right to Information.
75. Mention the type of patents.
76. Define copyright.
77. Define patents.
78. Give the criteria for patenting of inventions.
79. Define trademark as per IPR Act.