Download PTU (I.K. Gujral Punjab Technical University Jalandhar (IKGPTU) M.Pharma 2020 March (Master of Pharmacy) 2nd Sem 74946 Clinical Research And Pharmacovigilance Previous Question Paper
Roll No. Total No. of Pages : 01
Total No. of Questions : 06
M.Pharmacy (Pharmacology) (Sem.?2)
CLINICAL RESEARCH & PHARMACOVIGILANCE
Subject Code : MPL-204T
M.Code : 74946
Time : 3 Hrs. Max. Marks: 75
INSTRUCTIONS TO CANDIDATES :
1. Attempt any FIVE questions out of SIX questions.
2. Each question carries FIFTEEN marks.
1. a) Outline the requirements for a sterile product manufacturing plant. Indicate various
areas with the help of an illustration. (7.5)
b) Describe the constitution of IRB. Mention the functions of IRB. (7.5)
2. a) Write a note on cross sectional observation studies. (7.5)
b) Comment on the responsibilities of study coordinator of a clinical trial. (7.5)
3. a) What is an investigator brochure? Outline the contents of this brochure and mention the
purpose of each entry in the form. (7.5)
b) What is ADR? Give five examples of ADRs. How are ADRs detected and reported?
Outline the format used for this purpose. (7.5)
4. Outline the importance of safety monitoring in clinical trials. Give a detailed account of
safety monitoring in clinical trials. (15)
5. Give a detailed account of passive and active surveillance in pharmacovigilance. Outline
the steps involved in each. (15)
6. Write notes on (any three) : (5 ? 3 = 15)
a) Pharmacoeconomics
b) Responsibilities of a CRO
c) Pharmacovigilance in hospitals
d) International classification of diseases
NOTE : Disclosure of Identity by writing Mobile No. or Making of passing request on any
page of Answer Sheet will lead to UMC against the Student.
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This post was last modified on 31 March 2020