Pharmaceutical Jurisprudence and Ethics Important Question
Pharmaceutical Jurisprudence and Ethics Question Short Answers – 02 Marks:
Q 1. Add a note on the Drugs Enquiry Committee.
Q 2. What is Hathi Committee?
Q 3. What is Mudaliar Committee?
Q 4. Explain the role of the pharmacist in relation to his trade.
Q 5. Explain the role of the pharmacist in relation to his job.
Q 6. Explain the role of the pharmacist in relation to his profession.
Q 7. Define the term Drug under D & C Act.
Q 8. Define the term Adulterated drug under D & C Act.
Q 9. Define the term Spurious drug under D & C Act.
Q 10. Define the term Misbranded drug under D & C Act.
Q 11. Define Schedule X and give 2 examples of drugs.
Q 12. Define Schedule H and give 2 examples of drugs.
Q 13. Write the objectives of the Medicinal and Toilet Preparations Act.
Q 14. Define i.) Spirit ii.) Denatured Alcohol under M & TP Act.
Q 14. Define i.) Lunatic; ii.) RMP under MTP Act.
Q 15. Write the conditions for termination of Pregnancy.
Q 16. Write the objectives of pharmaceutical policy 2002.
Q 17. Define the term MAPE.
Q 18. Write the formula for calculating the retail price of a formulation.
Q 19. Add a note on NLEM.
Q 20. Write the salient features of the Hatch Waxman Act 1984.
Q 21. Write a note on generic drugs with two examples.
Q 22. Write the constitution of IAEC.
Q 23. Write the functions of IAEC.
Q 24. List the conditions required for breeding animals for experimentation.
Q 25. Add a note on NDA.
Q 26. Add a note on ANDA
Q 27. Revocation of Patents
Q 28. Write about the recommendations of DEC.
Q 29. Write a note on Joint State Pharmacy Council.
Q 30. Reproduce Pharmacist’s Oath.
Q 31. What are the labeling requirements for i) Colored Preparations ii.) Medicine for External Use
Pharmaceutical Jurisprudence and Ethics Important Question Short Essay – 05 Marks:
Q 1. Write about the constitution and functions of the PCI
Q 2. Explain about ER. Write the salient features of ER 91.
Q 3. Write the constitution and functions of the state pharmacy council.
Q 4. How is the first register prepared and maintained?
Q 5. Explain in brief about the registration of pharmacists.
Q 6. Write in brief about the layout of a bonded laboratory.
Q 7. Write a note on the warehousing of alcoholic preparations.
Q 8. Discuss the provisions relating to the manufacture of ayurvedic and homeopathic medicines containing alcohol
Q 9. Explain in brief about manufacturing alcoholic preparations under M & TP Act.
Q 10. Write the operations controlled by the Central and State Governments under NDPS Act.
Q 11. Discuss the cultivation of opium under the NDPS Act.
Q 12. Explain in brief about offenses and penalties under NDPS Act.
Q 13. Explain in brief the import and export of Narcotic drugs and Psychotropic substances under the NDPS Act.
Q 14. Discuss the advertisements exempted under the Drugs and Magic Remedies Act.
Q 15. Discuss the advertisements prohibited under the Drugs and Magic Remedies Act.
Q 16. Write the general procedures with timelines for obtaining a patent.
Q 17. What are the qualifications required for appointing a Government Analyst? What are the functions of the Government Analyst?
Q 18. Write the labeling requirements of medicines for internal use with a model label.
Q 19. Explain in detail about Schedule N.
Q 20. Write a note on the loan license and repackaging license.
Q 21. What is the subsequent register and how is it prepared?
Q 22. What are the grounds on which the name of a pharmacist can be removed from the Central Register? Write about the rights of pharmacists and the procedure to appeal against it.
Q 23. Write about Central Drugs Laboratory and its role.
Q 24. Write about the power of entry, search, and seizure without a warrant under the NDPS Act.
Jurisprudence Important Question Long Essay – 10 Marks:
Q 1. Describe the constitution and functions of a) DTAB b) DCC
Q 2. What are the conditions for the grant of a license to manufacture drugs other than those specified in Schedule C and C1 of D and C Rules 1945?
Q 3. Explain the different licenses issued for the sale of drugs. Describe the general procedure for a license stating the conditions to be satisfied.
Q 4. Explain in detail about Schedule M (GMP) under D & C Act.
Q 5. Explain in detail about Schedule Y under D & C Act.
Q 6. What are the qualifications for appointment as a drugs inspector? Describe the powers and duties of the drug inspector appointed under the D & C Act.
Q 7. Enumerate in detail the classes of drugs totally prohibited and permitted to be imported under license or permission under D & C Act.
Q 8. Discuss the penalty for manufacturing and sale of drugs in contravention of the D & C Act 1940.
Q 9. Explain in detail about manufacturing, import, and sale of ayurvedic/homeopathic medicines.
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