Pharmaceutical Jurisprudence PYQs – Set 89
Subject : Pharmaceutical Jurisprudence
1761. Chairman of DTAB is:
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2016
1762. Efficiency of drug is checked in a modest population in
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2016
1763. What is the required floor area for running a pharmacy for wholesale or distribution?
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2016
1764. Which of the following methods is used to determine whether a process functions properly for its intended use?
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2016
1765. Drugs (price control) order 1995 and related orders are enforced by
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2016
1766. In order to make a generic substitution, a pharmacist must also act as a hydrogen bond acceptor by:
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2016
1767. The clinical trial registry in India is maintained by
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2016
1768. Which term describes "the degree to which a set of inherent properties of a product system fulfills requirements"
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2016
1769. Within how many days should a pharmacist dispense diluted aqueous mixtures?
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2016
1770. TGA is the regulatory body of which country?
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2016
1771. Match the schedules with the particulars they describe: 1. Schedule T, 2. Schedule U, 3. Schedule V, 4. Schedule Y
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2016
1772. A clinical trial is being conducted with 1500 volunteers over a period of 2 years as per protocol. The trial is in which phase?
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2016
1773. If the drug substance has been substituted wholly or in part by another drug or substance, it is called as
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2016
1774. Highlighting differences among brands within the same product category is called
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2016
1775. Chapter IV of which law states that experiments on animals are avoided wherever possible if alternative teaching devices are available
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2016
1776. According to the first schedule of the Drugs and Cosmetics Act, 1940, the book under the Siddha system of medicine is
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2016
1777. Pharmaceutical alternatives possess
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2016
1778. Which of the following formulations under the ASU system are offered an infinite shelf life as per the D&C Act?
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2016
1779. Phase 0 studies mean
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2016
1780. WIPO is the specialized agency of the United Nations. It promotes protection of
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2016
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