Pharmaceutical Jurisprudence – Important Questions with Answers – Unit Wise Guide (B pharma 5th semester solved)

Pharmaceutical Jurisprudence – Important Questions with Answers – Unit Wise Guide (B pharma 5th semester solved)

Section A

Unit-I Questions

  1. What do you mean by misbranded drug?
  2. Define adulterated drug.
  3. Define spurious drug.
  4. Define the term adulterated, misbranded, and spurious drugs according to the Drugs and Cosmetics Act.
  5. What do you mean by import of drugs?
  6. Define bonded laboratory.
  7. Write a note on Repacking License.
  8. What are adulterated and spurious drugs?
  9. What are the objectives of the Drugs and Cosmetics Act, 1940?

Unit-II Questions

  1. What is Schedule G?
  2. What is Schedule M?
  3. What are Schedule G and Schedule N?
  4. What are Schedule J and Schedule M?
  5. Write in detail about Schedule M.
  6. Write about Schedule M and Schedule G.
  7. Define the term retail sale.
  8. Define the term restricted license.
  9. What is DTAB?
  10. Write the functions of Drugs Technical Advisory Board.
  11. Write the functions and duties of Drug Inspector.

Unit-III Questions

  1. What is the objective of the Pharmacy Act?
  2. Give four functions of the Pharmacy Council of India.
  3. Define registered pharmacist.
  4. Define medical practitioner.
  5. Write the objective of the Medicinal and Toilet Preparations Act, 1955.
  6. Write the objective of the Narcotic Drugs and Psychotropic Substances Act, 1985.
  7. Define the term poison.
  8. Define coca leaf.
  9. Define prepared opium.
  10. Define narcotic drugs. Give examples.
  11. Give examples of any four narcotic drugs.
  12. Define psychotropic substance.
  13. Write the difference between Charas, Ganja, and Bhang.

Unit-IV Questions

  1. Define magic remedy.
  2. Define advertisement.
  3. List two offences and penalties under the Cruelty to Animals Act, 1961.
  4. List two offences and penalties under the Drug and Magic Remedies Act.
  5. What is DPCO?
  6. Write the formula for calculation of retail price of a drug.
  7. What are CPCSEA guidelines?
  8. Write the full form of CPCSEA and IAEC.
  9. Write the full form of CPCSEA and NLEM.
  10. Write the full form of CPCSEA, IAEC, and NLEM.
  11. What is NLEM?

Unit-V Questions

  1. Define Pharmaceutical Jurisprudence.
  2. What do you mean by jurisprudence?
  3. What are the objectives of the Patent Act?
  4. What are the objectives of the Trademark Act?
  5. What are the objectives of the Right to Information Act?
  6. What is Hathi Committee?
  7. What do you mean by forensic pharmacy?
  8. Write a short note on patent.
  9. What is Intellectual Property Rights?
  10. Write in brief about the code of pharmaceutical ethics.
  11. Write the pharmacist’s oath.
  12. Copyright Act, Poisons Act, Trademark Act, Medical Termination of Pregnancy Act, and Drug and Magic Remedies Act were passed in which year?

Section B

Unit-I Questions

  1. Write in detail about import of drugs and classes of drugs prohibited from import under the Drugs and Cosmetics Act.
  2. Explain in detail the classes of drugs that can be imported under license, procedure for application, conditions, and suspension and cancellation of import license under the Drugs and Cosmetics Act.
  3. Write a note on licenses required for wholesale sale of drugs under the Drugs and Cosmetics Act.
  4. Discuss licenses required for wholesale and retail sale of drugs, including offences and penalties under the Drugs and Cosmetics Act, 1940 and Rules, 1945.
  5. Write in detail about Schedule M (GMP) under the Drugs and Cosmetics Act, 1940.

Unit-II Questions

  1. Write in brief the constitution and functions of the Drugs Technical Advisory Board (DTAB).
  2. Explain education regulations and registration of pharmacists under the Pharmacy Act.

Unit-III Questions

  1. Write about Pharmaceutical Education Regulations under the Pharmacy Act.
  2. Write in detail about Pharmacy Council of India (PCI), its constitution, and functions.
  3. Explain the Pharmacy Act, 1948 with reference to constitution and functions of PCI, State Pharmacy Council, and registration of pharmacists.
  4. Write a note on qualification of a medical practitioner and places where pregnancy may be terminated.
  5. Explain in detail the Medical Termination of Pregnancy Act.
  6. Describe the classes of drugs which can be imported, exported, and transshipped under the Narcotic Drugs and Psychotropic Substances Act.
  7. Write the constitution and functions of the Narcotic and Psychotropic Consultative Committee.

Unit-IV Questions

  1. Discuss in brief CPCSEA guidelines for the breeding and stocking of animals.
  2. What is the National List of Essential Medicines (NLEM)? Write the objectives of Drug Price Control Order (DPCO).

Unit-V Questions

  1. Write in detail about pharmaceutical legislations.
  2. Discuss in detail the Right to Information Act (RTI).
  3. Write about the code of pharmaceutical ethics and the Pharmacist’s Oath.

Section C

Unit-I Questions

  1. Discuss manufacturing of drugs for examination, test or analysis, and loan license.
  2. Discuss the classes of drugs and cosmetics prohibited from import and drugs imported under license.
  3. Discuss the conditions for grant of license for manufacture of drugs, manufacture for test, and loan license.
  4. Explain the procedure for obtaining a license to manufacture medicinal and toilet preparations containing alcohol or other narcotic substances.
  5. Write a note on the Drugs and Cosmetics Act, 1940 and explain the requirements for obtaining a retail license.
  6. Write the requirements for obtaining a retail license under the Drugs and Cosmetics Act, 1940.
  7. Explain loan license and repacking license.
  8. Write brief about manufacturing outside bond.
  9. Illustrate the sale of drugs under the Drugs and Cosmetics Act.
  10. Write in brief about wholesale and retail sale of drugs.
  11. Write offences and penalties related to the sale of drugs.

Unit-II Questions

  1. Write a note on Schedule G, Schedule H, Schedule M, and Schedule N.
  2. Give specimen labels for Schedule H and Schedule X drugs with suitable examples.
  3. Give a detailed account of labeling and packing of drugs.
  4. Discuss the GMP guidelines mentioned under Schedule M.
  5. Write in brief about Schedule M.
  6. Explain the qualifications, powers, and duties of Drug Inspector.
  7. Write a note on the constitution and functions of the Drugs Technical Advisory Board (DTAB).

Unit-III Questions

  1. Write the constitution and functions of the Narcotic and Psychotropic Consultative Committee.
  2. Describe the functions of the Narcotic and Psychotropic Consultative Committee.
  3. Describe the provisions for registration and removal of names under the Pharmacy Act, 1948.
  4. Write a note on the constitution and functions of the Pharmacy Council of India (PCI).
  5. Explain the Pharmacy Act, 1948 with reference to State Pharmacy Council, Joint State Pharmacy Council, and registration of pharmacists.
  6. Write a note on registration of pharmacists.
  7. Write a note on the State Pharmacy Council and Joint State Pharmacy Council and their functions.
  8. Discuss the role of the pharmacist as a member of the health care team.
  9. Define the role of the pharmacist and explain the procedure for pharmacist registration.
  10. Discuss the rules relating to export, import, and transshipment of narcotic drugs.
  11. Write terms and conditions for the cultivation, collection, and production of opium.
  12. Write a note on the Narcotic Drugs and Psychotropic Substances Act, 1985 and its Rules.

Unit-IV Questions

  1. Write a note on CPCSEA guidelines for breeding and stocking of animals.
  2. Write the objectives of the Prevention of Cruelty to Animals Act.
  3. Enumerate the retail price and ceiling price of scheduled formulations.
  4. Write a note on retail price of formulations.
  5. Write in detail about the Drug Price Control Order (DPCO), 1995.

Unit-V Questions

  1. Explain various types of Intellectual Property Rights (IPR).
  2. Write a short note on Intellectual Property Rights (IPR).
  3. Write in detail about pharmaceutical legislations.
  4. Write about the code of pharmaceutical ethics and the Pharmacist’s Oath.
  5. What are the Hathi Committee and Bhore Committee?
  6. Write a brief review of pharmaceutical legislation.
  7. Define advertisement and explain exempted and prohibited advertisements under the Drug and Magic Remedies Act.
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