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Pharmaceutical Jurisprudence MCQ with Answer
Pharmaceutical Jurisprudence is the study of rules and regulations of pharmacy, pharmacy practice, and also relating to drugs and pharmaceuticals.
Let’s explore some pharmaceutical jurisprudence MCQs for each answer:
1.For parenteral preparation in glass containers minimum area required is
a) 250 square meters
b) 400 square meters
c) 500 square meters
d) 150 square meters
Ans: a) 250 square meters
2.In State Pharmacy Council all following are ex officio members except.
a) President of India
b) Chief Administrator medical officer of state
c) The officer in charge of drugs control organization
d) Government Analyst
Ans: a) President of India
3.Schedule X of Drugs and Cosmetics Act comprises
a. List of incurable diseases
b. Guidelines for clinical Trials
c. List of generic drugs
d. None of the above
Ans: d) None of the above
4.As per D and C Act “Schedule N” is related with
a. List of maximum equipments for efficiently running pharmacy
b. Area for opening retail pharmacy
c. List of minimum equipments for efficiently running pharmacy
d. Area required to open wholesale drug store
Ans: c) List of minimum equipments for efficiently running pharmacy
5. As per D & C Act “Schedule FF” is related with
a. Parenteral preparation
b. Ointment formulation
c. Skin cosmetic preparation
d. Ophthalmic preparation
Ans: d) Ophthalmic preparation
6.Which of the following is prohibited to be imported?
a. Toilet preparations
b. Ayurvedic drugs
c. Schedule ‘C’ ‘G’ drugs
d. Misbranded drugs
Ans: d) Misbranded drugs
7.Hatch Waxman Act is related to
a. Banned drugs
b. Over the counter drugs
c. Dangerous drugs Act
d. Spurious drugs Act
Ans: d) Spurious drugs Act
8.The first edition of India Pharmacopoeia was published in the year :
a. 1940
b. 1950
c. 1955
d. 1985
Ans: c) 1955
9. Coca, opium and hemp come under:
a. Insecticide Act
b. Poisons Act
c. Dangerous Drug Act
d. Spurious Drug Act
Ans: c) Dangerous Drug Act
10.Pharmacy Council of India (PCI) is reconstituted:
a. Every 2 year
b. Every 3 year
c. Every 5 year
d. Every 6 year
Ans: c) Every 5 year
11.In Phase-2 trial following number of patient should be studied
a. 10-12 patients
b. 1-10 patients
c. 100 patients
d. 500 patients
Ans: a) 10-12 patients
12.Purpose of Phase-3 trial is
a. To determine maximum tolerated dose in humans, Pharmacodynamics effects, Adverse effect.
b. Determine Possible therapeutic uses, Effective doses range
c. Efficacy and Safety of drug in longer number of patients (500 patients)
d. Long time adverse effects aster marketing drug
Ans: c) Efficacy and Safety of drug in longer number of patients (500 patients)
13.Standard for mechanical contraceptive comes under Schedule ………………as per D & C Act
a. R
b. R1
c. S
d. O
Ans: b) R1
14.Patent Act is established in
a. 1948
b. 1940
c. 1970
d. 1919
Ans: c) 1970
15.Pack size of drug is covered under
a. Schedule P
b. Schedule P1
c. Schedule R
d. Schedule O
Ans: b) Schedule P1
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