Pharmaceutical Jurisprudence PYQs – Set 90

By Atul Sahu • Pharmaceutical Jurisprudence, Subject Wise PYQs

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

A. Licensing authority B. Drug inspectors C. Drugs Consultative Committee D. Customs collectors

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

A. 30 B. 40 C. 48 D. 56

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

A. New product B. New process C. New use of existing drug D. New process for existing drug

1784. Vials and bottles are regularly not subjected to which test?

Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018

A. Sterility test B. Clarity test C. Leaker (chamber) test D. Pyrogen test

1785. The number of subjects required in a phase 1 clinical trial is typically:-

Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018

A. 20 to 100 B. Up to several hundred C. 300 to 3,000 D. Several thousands

1786. Under the Drugs and Cosmetic Act, 1940, drug inspectors’ powers are defined in:

Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018

A. 20 B. 21 C. 22 D. 23

1787. India’s first Central Drug Laboratory was established in?

Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018

A. Mumbai B. Lucknow C. Kolkata D. Hyderabad

1788. Which of the following USP glass types is not suitable for parenteral packaging?

Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018

A. Type I B. Type II C. Type III D. Type IV

1789. When is a New Drug Application (NDA) typically submitted?

Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018

A. After animal studies B. After phase III clinical trials C. After phase IV clinical trials D. After preclinical studies

1790. Which of the following best defines an orphan drug?

Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018

A. A drug for orphan children B. A drug for common diseases C. A drug for cost-effective therapy D. A drug for rare diseases

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

A. Q1A (R2) B. Q1B C. Q1D D. Q1E

1792. Given two statements regarding rubber stoppers and pyrogen control, which is correct?

Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018

A. Both statements are correct B. Both statements are incorrect C. Statement I is correct but Statement II is incorrect D. Statement I is incorrect but Statement II is correct

1793. Who is the primary source of information for doctors' prescribing behavior?

Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018

A. Competitor B. Wholesaler C. Fellow doctor D. Retailer

1794. Schedule 'O' governs standards for which aspect of drug manufacturing?

Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018

A. Disinfectant fluids B. List of equipment to run a pharmacy C. Shelf-life (expiry) of drugs D. Manufacturing and analytical records

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

A. PART-IV B. PART-IB C. PART-IC D. PART-ID

1796. Schedule T of Drugs and Cosmetics Rules, 1945 deals with:

Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018

A. GMP for Homeopathy medicine B. GMP for ASU drugs C. GLP and requirement of premises and equipments D. GMP for Pharmaceutical product

1797. Central Government approved factory premises where Opium alkaloids are processed is situated at:

Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018

A. Ghazipur and Kota B. New Delhi And Ghaziabad C. Neemuch and Ghazipur D. Gwalior and Kota

1798. The term of a patent granted under Indian Patent’s Act is:

Pharmaceutical Jurisprudence • Drugs and Cosmetics Act, 1940 • GPAT 2018

A. 40 Years B. 10 Years C. 30 Years D. 20 Years

1799. As per US FDA, NDA’s for new chemical entities are classified as either :

Pharmaceutical Jurisprudence • FDA NDA review types • GPAT 2018

A. ‘P’ for product review or ‘S’ for standard review B. ‘P’ for priority review or ‘S’ for standard review C. ‘P’ for product review or ‘S’ for safety review D. ‘P’ for priority review or ‘S’ for safety review

1800. Which substance is exempt from import licensing?

Pharmaceutical Jurisprudence • Import Licensing & Exemptions • GPAT 2018

A. Insulin B. Etoposide C. Lactose D. Glutethimide

Disclaimer for MCQ Quiz
The questions in this MCQ quiz are intended solely for educational purposes. While we strive to ensure accuracy, the information may not always be up-to-date or complete. The creators are not liable for any errors or consequences. Verify any information before relying on it for critical decisions.

इस MCQ क्विज़ के प्रश्न केवल शैक्षिक उद्देश्यों के लिए हैं। हम सामग्री की सटीकता सुनिश्चित करने का प्रयास करते हैं, फिर भी जानकारी हमेशा अद्यतित या पूर्ण नहीं हो सकती। निर्माता किसी भी परिणाम के लिए जिम्मेदार नहीं हैं। कृपया किसी भी महत्वपूर्ण निर्णय से पहले स्वतंत्र रूप से जांचें।
https://www.growuppharma.in
यदि कोई गलती है या सुझाव हो तो ईमेल करें: growuppharmacy@gmail.com

Leave a Comment Cancel Reply