Pharmaceutical Jurisprudence PYQs – Set 88
Subject : Pharmaceutical Jurisprudence
1741. Consumer who are loyal to two-three brands are considered as :
Pharmaceutical Jurisprudence • Brand loyalty segments • GPAT 2019
1742. Which of the following is considered as differentiated product ?
Pharmaceutical Jurisprudence • Branded vs generic • GPAT 2019
1743. GMP regulation are pertaining to minimum requirements to be met by industry when :
Pharmaceutical Jurisprudence • cGMP (21 CFR 211) • GPAT 2019
1744. Post-marketing safety studies are conducted in which phase?
Pharmaceutical Jurisprudence • Clinical Trial Phases • GPAT 2019
1745. For depot injections (released over weeks/months), which study design is used?
Pharmaceutical Jurisprudence • Clinical Trial Phases & Designs • GPAT 2019
1746. Phase zero studies are best described as a/an:
Pharmaceutical Jurisprudence • Clinical Trial Regulations • GPAT 2019
1747. How customer’s bias about the product will influence the marketing communication?
Pharmaceutical Jurisprudence • Complete Subject • GPAT 2019
1748. As per the definition of the D and C Act, Gudakhu (rubbed on teeth) is considered as:
Pharmaceutical Jurisprudence • Cosmetics regulation • GPAT 2019
1749. Choose the CORRECT statement with respect to “The Pharmacy Act, 1948 :
Pharmaceutical Jurisprudence • Course approval • GPAT 2019
1750. Drug products that contain the same therapeutic moiety but as different salts, esters, or complexes are called
Pharmaceutical Jurisprudence • Drug equivalence categories • GPAT 2019
1751. Standards under the D & C Act1940 for drugs imported, manufactured, stocked, and exhibited for sale are covered under
Pharmaceutical Jurisprudence • Drug scheduling • GPAT 2019
1752. Which of the following drug comes under Schedule C?
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2019
1753. Ethics for pharmacists are put forth by:
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2019
1754. Opium, cocoa, and poppy straw are given in which schedule?
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2019
1755. According to Schedule 'Y' of the Drugs and Cosmetics Act, which statement regarding animal toxicity studies is incorrect?
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2019
1756. List of drugs governed by special provisions is included in which schedule?
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2019
1757. A pharmaceutical company plans to market a generic version of a drug whose patent has expireD : Which type of documentation must be submitted to the FDA?
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2019
1758. A clinical trial is being conducted with 1500 volunteers over 2 years. The trial is in which phase?
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2019
1759. The chairman of the Investigational New Drug (IND) committee in India is
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2019
1760. Adverse Drug Event reporting is the responsibility of all of the following EXCEPT
Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2019
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