Pharmaceutical Jurisprudence PYQs – Set 91
Subject : Pharmaceutical Jurisprudence
1801. Which form is used to import small quantities of drugs for personal use?
Pharmaceutical Jurisprudence • Import Licensing & Forms • GPAT 2021
1802. Which drug can be imported without a license?
Pharmaceutical Jurisprudence • Import licensing exemptions • GPAT 2021
1803. In which year did India sign the General Agreement on Tariffs and Trade (GATT) including TRIPS?
Pharmaceutical Jurisprudence • International trade agreements • GPAT 2021
1804. Under ISO, the standard for quality system model for quality assurance in production, installation, and servicing is given under
Pharmaceutical Jurisprudence • ISO 9002 • GPAT 2021
1805. As per the Drugs and Cosmetics Act1940, if a drug is not labelled in the prescribed manner it is classified as
Pharmaceutical Jurisprudence • Misbranded drugs • GPAT 2021
1806. As per the Medical Termination of Pregnancy Act and rules, the safe custody of “Forms” is with :
Pharmaceutical Jurisprudence • MTP Act forms • GPAT 2021
1807. Penalty for the cultivation of any cannabis plant to produce, sell, purchase, transport in contravention of Narcotic Drugs and Psychotropic substances Act and Rules on first conviction is
Pharmaceutical Jurisprudence • NDPS Act penalties • GPAT 2021
1808. In India the patent office has its head office at Kolkata and branch offices at :
Pharmaceutical Jurisprudence • Patent office locations • GPAT 2021
1809. According to the Pharmacy Act, what is the total number of PCI ex-officio members?
Pharmaceutical Jurisprudence • Pharmacy Act, 1948 • GPAT 2021
1810. Who has the power to fix the ceiling price of scheduled formulations:
Pharmaceutical Jurisprudence • Pharmacy Act, 1948 • GPAT 2021
1811. The ‘Up-and-Down’ method for LD50 determination is described in which OECD guideline?
Pharmaceutical Jurisprudence • Preclinical Toxicology Guidelines • GPAT 2021
1812. To create a successful new product, a company must understand consumers, markets, and competitors and develop a/an
Pharmaceutical Jurisprudence • Product Development • GPAT 2021
1813. Which product life-cycle phase indicates market saturation?
Pharmaceutical Jurisprudence • Product life‑cycle • GPAT 2021
1814. The objective of an audit is to:
Pharmaceutical Jurisprudence • Quality Assurance & Auditing • GPAT 2021
1815. Sigma minus method is used in the assessment of:
Pharmaceutical Jurisprudence • Quality Assurance & Auditing • GPAT 2021
1816. Regarding DTAB: Is DCGI its chairman and does it have 8 ex-officio members?
Pharmaceutical Jurisprudence • Regulatory Bodies & Authorities • GPAT 2021
1817. Who was the Chairman of the Drugs Enquiry Committee established in 1927?
Pharmaceutical Jurisprudence • Regulatory committees • GPAT 2021
1818. Headquarters of Bureau of Indian Standards is situated at:
Pharmaceutical Jurisprudence • Regulatory Compliance • GPAT 2021
1819. What is the name of the floor on which production work is done rather than administration?
Pharmaceutical Jurisprudence • Regulatory Compliance • GPAT 2021
1820. The 'Compendium of Pharmaceuticals and Specialties' is published by:
Pharmaceutical Jurisprudence • Regulatory Publications • GPAT 2021
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