Pharmaceutical Jurisprudence PYQs – Set 90
Subject : Pharmaceutical Jurisprudence
1781. Which of the following agencies is not classified as an ‘executive agency’ for administration of the act under the provision of Drugs and Cosmetics Act 1940?
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018
1782. As per Factories Act 1948, in Chapter VI dealing with working hours of adults, no adult worker shall be required or allowed to work in a factory for more than __ hours in a week.
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018
1783. Which of the following is not patentable in India as per The Patents Act 1970?
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018
1784. Vials and bottles are regularly not subjected to which test?
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018
1785. The number of subjects required in a phase 1 clinical trial is typically:-
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018
1786. Under the Drugs and Cosmetic Act, 1940, drug inspectors’ powers are defined in:
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018
1787. India’s first Central Drug Laboratory was established in?
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018
1788. Which of the following USP glass types is not suitable for parenteral packaging?
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018
1789. When is a New Drug Application (NDA) typically submitted?
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018
1790. Which of the following best defines an orphan drug?
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018
1791. Which ICH guideline provides the general requirements for stability testing of new drug substances and products?
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018
1792. Given two statements regarding rubber stoppers and pyrogen control, which is correct?
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018
1793. Who is the primary source of information for doctors' prescribing behavior?
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018
1794. Schedule 'O' governs standards for which aspect of drug manufacturing?
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018
1795. Specific requirements for the manufacture of sterile products and parenteral preparations are detailed in which part of Schedule-M?
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018
1796. Schedule T of Drugs and Cosmetics Rules, 1945 deals with:
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018
1797. Central Government approved factory premises where Opium alkaloids are processed is situated at:
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018
1798. The term of a patent granted under Indian Patent’s Act is:
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018
1799. As per US FDA, NDA’s for new chemical entities are classified as either :
Pharmaceutical Jurisprudence • FDA NDA review types • GPAT 2018
1800. Which substance is exempt from import licensing?
Pharmaceutical Jurisprudence • Import Licensing & Exemptions • GPAT 2018
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