Question

DST

05 Mar 2024
Answer :
Word Count : 563
  1. What is the primary role of the Drug Regulatory Authority?
    A) Approving clinical trials
    B) Ensuring drug safety and efficacy
    C) Manufacturing drugs
    D) Marketing drugs
    Answer: B) Ensuring drug safety and efficacy

  2. Which document is required for the registration of a new drug?
    A) Clinical trial approval
    B) New Drug Application (NDA)
    C) Good Manufacturing Practices (GMP) certification
    D) Drug Master File (DMF)
    Answer: B) New Drug Application (NDA)

  3. What is the primary purpose of the Good Manufacturing Practices (GMP) guidelines?
    A) To ensure the efficacy of drugs
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