Pharmaceutical Jurisprudence MCQ

Test your knowledge with important Pharmaceutical Jurisprudence MCQ and their applications. These MCQs are beneficial for competitive exams too. Explore 30 + more Pharmaceutical Jurisprudence MCQs at Bissoy

• The Latin word jurisprudentia denotes . . . . . . . .
  ক

  Knowledge of guidelines

  খ

  Knowledge of law

  গ

  Knowledge of ethics

  ঘ

  Knowledge of rules
• List of coal tar colours permitted to be used in cosmetics is covered under . . . . . . . .
  ক

  Schedule O

  খ

  Schedule P

  গ

  Schedule Q

  ঘ

  Schedule R
• Alcoholic preparations can be stored in a ware house for a maximum period of
  ক

  6 years

  খ

  5 years

  গ

  3 years

  ঘ

  2 years
• Pharmacy, Act 1948 provides for the constitution of central council under . . . . . . . . by central government.
  ক

  Section 3

  খ

  Section 3 of Chapter 1

  গ

  Section 4

  ঘ

  Section 4 of Chapter 1
• Second schedule to act of D & C act deals with . . . . . . . .
  ক

  Standard for Homeopathic system

  খ

  Standard for Unani system

  গ

  Standards for imported & manufactured drug for sale

  ঘ

  Standards for supernatural products
• TGA is a regulatory body of which country?
  ক

  Australia

  খ

  U. K.

  গ

  Canada

  ঘ

  Europe
• Education regulation prepared under subject to provision of . . . . . . . . of pharmacy act, 1948
  ক

  Section 3

  খ

  Section 4

  গ

  Section 10

  ঘ

  Section 3A
• Ergot alkaloids belong to schedule
  ক

  P

  খ

  G

  গ

  H

  ঘ

  S
• Select the percentage content of morphine in opium
  ক

  Less than 0.2%

  খ

  More than 0.3%

  গ

  More than 0.4%

  ঘ

  More than 0.2%
• National Board of Accreditation (NBA) was established in the year
  ক

  1954

  খ

  1994

  গ

  1957

  ঘ

  1988
• Blood & blood products are governed by which schedule of the D & C act
  ক

  Schedule B

  খ

  Schedule C & C1

  গ

  Schedule G

  ঘ

  Schedule W
• Manufacture in relation to any drug does not include the process of 5
  ক

  Ornamenting

  খ

  Labelling

  গ

  Packing

  ঘ

  Compounding
• Specific requirements for mainu-facture of sterile products and parental preparations are prescribed in which of the following parts of the Schedule M?
  ক

  Part IA

  খ

  Part IB

  গ

  Part IC

  ঘ

  Part ID
• Which one is the principle of Community?
  ক

  Respecting the consumer's autonomy and rights

  খ

  Conducting the pharmacy business ethically and professionally

  গ

  Demonstrating a commitment to the development

  ঘ

  Upholding the reputation and public trust of the profession
• Advertisements of prescription drugs are meant for:
  ক

  Physician

  খ

  Distributor

  গ

  Patient

  ঘ

  Retail Pharmacy
• Which of the following is an ayurvedic preparation containing self generated alcohol?
  ক

  Asava

  খ

  Gutika

  গ

  Lehya

  ঘ

  Ghrita
• The term of every patent in India is:
  ক

  10 years

  খ

  15 years

  গ

  20 years

  ঘ

  25 years
• Drug and cosmetics rules are divided into schedule.
  ক

  26

  খ

  23

  গ

  18

  ঘ

  28
• Pharmacy Act is established in
  ক

  1948

  খ

  1940

  গ

  1995

  ঘ

  1919
• Minimum period of training required for registration of pharmacist is
  ক

  100 hours

  খ

  500 hours

  গ

  300 hours

  ঘ

  800 hours
• What is the duration of renewal license periods for selling drugs?
  ক

  5 years

  খ

  3 years

  গ

  4 years

  ঘ

  6 years
• Drugs legally allowed to be sold over the counter without prescription of RMP are
  ক

  Schedule H drugs

  খ

  OTC drugs

  গ

  Schedule G drugs

  ঘ

  All
• The number of persons elected for the Pharmacy Council of India from the teaching profession is
  ক

  Five

  খ

  Six

  গ

  Seven

  ঘ

  Eight
• A pharmacist seeks with justice in . . . . . . . . of health resources.
  ক

  Distribution

  খ

  Respect

  গ

  Integrity

  ঘ

  Dignity
• The minium required area to open a retail drug store is.
  ক

  15 sqm

  খ

  10 sqm

  গ

  40 sqm

  ঘ

  60 sqm
• Punishment for consumption of any narcotic drug or psychotropic substitute is
  ক

  Imprisonment up to six months or fine up to twenty thousand rupees or both

  খ

  Rigorous imprisonment up to six months or fine up to ten thousand rupees or both

  গ

  Imprisonment? up to two years or fine viip j to twenty thousand rupees or both

  ঘ

  Rigorous imprisonment up to one year or fine up to twenty thousand rupees or both
• Private testing laboratory for carrying out tests on drugs requires
  ক

  Form 32

  খ

  Form 31

  গ

  Form 30

  ঘ

  Form 36
• Central License Approving Authority (CLAA) is
  ক

  The Drugs Controller of India

  খ

  Chairman, DTAB

  গ

  Director, Central Drug laboratory

  ঘ

  State Drug Controller Authorities
• Period granted for the pharmaceutical industry to comply with the requirements of schedule L₁ is :
  ক

  1 year

  খ

  2 year

  গ

  3 year

  ঘ

  4 year
• The chairman of the investigational new drug (IND) committee in India is
  ক

  Drug controller general of India, Government of India

  খ

  Secretary, department of health research, Government of India

  গ

  Directorate general of health sciences, Government of India

  ঘ

  Secretary, department of biotechnology, government of India