Objectives of Prevention of Cruelty to Animals Act 1960 MCQs With Answer

Introduction: The Objectives of Prevention of Cruelty to Animals Act 1960 MCQs With Answer provide B.Pharm students a focused review of animal welfare, legal responsibilities and ethical standards in biomedical research. This introduction covers key objectives: prevent unnecessary pain and suffering, regulate animal experimentation, ensure proper housing, transport and humane treatment, and enforce licensing, inspection and penalties. It highlights oversight mechanisms such as the CPCSEA and Institutional Animal Ethics Committees, and promotes the 3Rs—Replacement, Reduction and Refinement—critical for pharmacology and toxicology work. Clear knowledge of these objectives aids responsible in vivo study design, compliance and patient safety. ‘Now let’s test your knowledge with 30 MCQs on this topic.’

Q1. What is a primary objective of the Prevention of Cruelty to Animals Act 1960?

  • To promote use of as many animals as possible in research
  • To prevent unnecessary pain, suffering and cruelty to animals
  • To prioritize economic benefits over animal welfare
  • To deregulate animal breeding

Correct Answer: To prevent unnecessary pain, suffering and cruelty to animals

Q2. Which of the following best describes the scope of the Act?

  • It applies only to laboratory rodents
  • It applies to animals used in research, transport, performance and general treatment across the country
  • It applies only to zoo animals
  • It only regulates pet ownership

Correct Answer: It applies to animals used in research, transport, performance and general treatment across the country

Q3. Which statutory body is responsible for oversight of experiments on animals under this Act?

  • Indian Council of Medical Research (ICMR)
  • Committee for the Purpose of Control and Supervision of Experiments on Animals (CPCSEA)
  • Drug Controller General of India (DCGI)
  • National Biodiversity Authority

Correct Answer: Committee for the Purpose of Control and Supervision of Experiments on Animals (CPCSEA)

Q4. What is the role of Institutional Animal Ethics Committees (IAECs) under the Act?

  • To promote commercial sale of laboratory animals
  • To review and approve animal study protocols and monitor welfare locally
  • To exempt institutions from following national rules
  • To fund animal research projects

Correct Answer: To review and approve animal study protocols and monitor welfare locally

Q5. Which ethical framework is explicitly promoted to minimize animal use in research?

  • The 4Ss: Sample, Scale, Schedule, Safety
  • The 3Rs: Replacement, Reduction and Refinement
  • The 7Ps: Plan, Perform, Publish, Protect…
  • The 2Cs: Control and Contain

Correct Answer: The 3Rs: Replacement, Reduction and Refinement

Q6. Before conducting an in vivo pharmacology experiment, a B.Pharm student must normally obtain:

  • Only verbal permission from a colleague
  • Approval from the Institutional Animal Ethics Committee (IAEC)
  • Approval from the local police station
  • No permission is required for student projects

Correct Answer: Approval from the Institutional Animal Ethics Committee (IAEC)

Q7. Which of the following is an objective related to housing and care under the Act?

  • Allowing overcrowding to reduce costs
  • Ensuring proper housing, nutrition, veterinary care and humane handling
  • Prohibiting any veterinary intervention
  • Mandating experimentation without rest

Correct Answer: Ensuring proper housing, nutrition, veterinary care and humane handling

Q8. How does the Act address transportation of animals?

  • It mandates unsafe transport to save time
  • It requires measures to prevent unnecessary suffering during transport
  • It does not mention transport at all
  • It forbids any transport under all circumstances

Correct Answer: It requires measures to prevent unnecessary suffering during transport

Q9. Which practice is encouraged as an alternative to animal use under the Act’s objectives?

  • Using unregulated human volunteers instead
  • Adopting validated non-animal methods like in vitro assays or computer modeling
  • Increasing animal numbers to ensure reproducibility
  • Using wild-caught animals for convenience

Correct Answer: Adopting validated non-animal methods like in vitro assays or computer modeling

Q10. What must an IAEC evaluate in a proposed animal experiment?

  • The color preferences of the research team
  • Scientific justification, pain minimization, number of animals and humane endpoints
  • Only the budget of the project
  • Whether the experiment will be profitable

Correct Answer: Scientific justification, pain minimization, number of animals and humane endpoints

Q11. Which statement about anesthesia and analgesia is consistent with the Act’s objectives?

  • Anesthesia should be avoided to observe natural pain responses
  • Appropriate anesthesia and analgesia must be used to minimize pain unless scientifically justified otherwise
  • Analgesia is optional and discouraged
  • Only sedatives, never analgesics, should be used

Correct Answer: Appropriate anesthesia and analgesia must be used to minimize pain unless scientifically justified otherwise

Q12. What is a humane endpoint in animal experimentation?

  • A point when researchers stop monitoring animals
  • The predefined condition at which an animal is removed from a study to prevent undue suffering
  • A requirement to extend suffering for statistical power
  • A deadline for publishing results

Correct Answer: The predefined condition at which an animal is removed from a study to prevent undue suffering

Q13. Which of the following actions is a legal consequence for cruelty under the Act?

  • Mandatory community service without fines
  • Prosecution which may include fines and/or imprisonment
  • Only informal warnings with no legal penalty
  • Immediate acquittal if the person claims ignorance

Correct Answer: Prosecution which may include fines and/or imprisonment

Q14. Who is generally responsible for appointing members of the CPCSEA or equivalent oversight bodies?

  • Private pharmaceutical companies
  • The central government or designated authority
  • Individual research students
  • Local animal breeders exclusively

Correct Answer: The central government or designated authority

Q15. Which of the following is NOT part of responsible record-keeping under the Act’s objectives?

  • Maintaining animal acquisition and health records
  • Keeping detailed experimental protocols and outcomes
  • Failing to document animal use to avoid scrutiny
  • Reporting adverse events to the oversight body

Correct Answer: Failing to document animal use to avoid scrutiny

Q16. What is the Act’s stance on performing animals in entertainment?

  • It seeks to regulate performance practices to prevent cruelty
  • It encourages unrestricted use of animals in entertainment
  • It mandates animals must be used for all public shows
  • It does not consider entertainment-related cruelty

Correct Answer: It seeks to regulate performance practices to prevent cruelty

Q17. For B.Pharm practicals involving animals, which step is essential to remain compliant?

  • Using animals without supervision to speed up learning
  • Obtaining IAEC approval, using minimum animals and following humane procedures
  • Purchasing any animal from unregistered dealers
  • Removing analgesia to observe full drug effects on pain

Correct Answer: Obtaining IAEC approval, using minimum animals and following humane procedures

Q18. Which committee inspects and monitors animal facilities to ensure compliance?

  • Institutional Finance Committee
  • CPCSEA or its designated inspectors
  • Student Council
  • Local sports association

Correct Answer: CPCSEA or its designated inspectors

Q19. What is the recommended approach when a validated non-animal method exists?

  • Prefer animal methods for traditional reasons
  • Use the non-animal method to replace animal testing when suitable
  • Ignore alternatives until regulators mandate them
  • Use both methods simultaneously to be safe

Correct Answer: Use the non-animal method to replace animal testing when suitable

Q20. Which of the following is a responsibility of institutions under the Act?

  • To minimize oversight and operate secretly
  • To establish IAECs, maintain records and ensure welfare standards
  • To outsource oversight to private marketing firms
  • To avoid training staff in humane animal care

Correct Answer: To establish IAECs, maintain records and ensure welfare standards

Q21. What should researchers do if an animal experiences unexpected severe pain during a study?

  • Continue the procedure to gather more data
  • Implement humane endpoint procedures and provide veterinary care
  • Ignore and hope it resolves
  • Hide the event from the IAEC

Correct Answer: Implement humane endpoint procedures and provide veterinary care

Q22. Which principle helps in reducing the number of animals used in experiments?

  • Randomly increasing sample sizes
  • Applying statistical power calculations and study design refinement
  • Repeating the same experiment multiple times unnecessarily
  • Using different species for each replicate

Correct Answer: Applying statistical power calculations and study design refinement

Q23. In the context of the Act, what does “refinement” mean?

  • Improving animal welfare by modifying procedures to minimize pain and distress
  • Refining laboratory chemicals to be more toxic
  • Refining budgets to reduce animal care
  • Refining publication drafts only

Correct Answer: Improving animal welfare by modifying procedures to minimize pain and distress

Q24. Who can lodge a complaint about suspected cruelty under the Act?

  • Only veterinarians
  • Any concerned person or organization
  • Only the head of the institution
  • Only governmental ministers

Correct Answer: Any concerned person or organization

Q25. Which of the following is an important documentation responsibility after completing an animal study?

  • Destroying all records immediately
  • Maintaining detailed experimental records and reporting outcomes to oversight bodies as required
  • Publishing results without disclosing animal use
  • Sharing animals with other labs without tracking

Correct Answer: Maintaining detailed experimental records and reporting outcomes to oversight bodies as required

Q26. Which option is NOT one of the 3Rs promoted under the Act’s objectives?

  • Replacement
  • Reduction
  • Refinement
  • Reuse

Correct Answer: Reuse

Q27. What is the purpose of licensing breeders and dealers under the Act?

  • To allow unmonitored trade of animals
  • To ensure animals used in research come from registered, inspected sources and are healthy
  • To increase the cost of acquiring animals for research
  • To permit export without welfare checks

Correct Answer: To ensure animals used in research come from registered, inspected sources and are healthy

Q28. How does the Act influence curriculum and training for B.Pharm students involved in animal work?

  • It mandates no training so students learn by trial and error
  • It emphasizes formal training in ethics, welfare, handling and humane techniques
  • It requires only online tests without hands-on guidance
  • It permits students to skip welfare training if supervised

Correct Answer: It emphasizes formal training in ethics, welfare, handling and humane techniques

Q29. What is one expected outcome when institutions follow the Act and its objectives?

  • Lower research quality due to restrictions
  • Improved animal welfare, scientific validity and public trust in research
  • Complete elimination of all animal research
  • Increased secrecy and reduced reporting

Correct Answer: Improved animal welfare, scientific validity and public trust in research

Q30. If a B.Pharm student suspects non-compliance in an animal facility, the best immediate action is to:

  • Conduct an independent experiment to verify
  • Report concerns to the IAEC or designated oversight authority following institutional procedures
  • Ignore it to avoid conflict
  • Post details publicly without following complaint procedures

Correct Answer: Report concerns to the IAEC or designated oversight authority following institutional procedures

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