Download PTU M-Pharma 2019 May 2nd Semester 74937 REGULATORY ASPECTS OF DRUGS and COSMETICS Question Paper

Download PTU (Punjab Technical University) M-Pharma (Master of Pharmacy) 2nd Semester 74937 REGULATORY ASPECTS OF DRUGS and COSMETICS Last 10 Years 2020, 2019, 2018, 2017, 2016, 2015, 2014, 2013, 2012, 2011 and 2010 Previous Question Papers.

1 | M-74937 (S31)-351

Roll No. Total No. of Pages : 02
Total No. of Questions : 06
M.Pharmacy(Regulatory Affairs) (2017 Batch) (Sem.?2)
REGULATORY ASPECTS OF DRUGS & COSMETICS
Subject Code : MRA-201T
M.Code : 74937
Time : 3 Hrs. Max. Marks : 75
INSTRUCTIONS TO CANDIDATES :
1. Attempt any FIVE questions out of SIX questions.
2. Each question carries FIFTEEN marks.

Q1. a) Discuss the regulation approval process for NDA. (8)
b) Explain the regulatory consideration for packaging and labeling of pharmaceutical in
EU. (7)
Q2. a) Write the full form of the following : (6)
a. CFR
b. DMF
c. CIS
d. ANDA
e. ASEAN
f. FFDCA
b) Discuss the regulatory requirement for manufacturing of pharmaceuticals in EU. (9)
Q3. Write a note on Any Three : (5?3)
a) CFR
b) WHO in relation to registration
c) ANDA
d) Labeling of pharmaceuticals in Japan
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1 | M-74937 (S31)-351

Roll No. Total No. of Pages : 02
Total No. of Questions : 06
M.Pharmacy(Regulatory Affairs) (2017 Batch) (Sem.?2)
REGULATORY ASPECTS OF DRUGS & COSMETICS
Subject Code : MRA-201T
M.Code : 74937
Time : 3 Hrs. Max. Marks : 75
INSTRUCTIONS TO CANDIDATES :
1. Attempt any FIVE questions out of SIX questions.
2. Each question carries FIFTEEN marks.

Q1. a) Discuss the regulation approval process for NDA. (8)
b) Explain the regulatory consideration for packaging and labeling of pharmaceutical in
EU. (7)
Q2. a) Write the full form of the following : (6)
a. CFR
b. DMF
c. CIS
d. ANDA
e. ASEAN
f. FFDCA
b) Discuss the regulatory requirement for manufacturing of pharmaceuticals in EU. (9)
Q3. Write a note on Any Three : (5?3)
a) CFR
b) WHO in relation to registration
c) ANDA
d) Labeling of pharmaceuticals in Japan
2 | M-74937 (S31)-351

Q4. Discuss in detail the organization and structure of EMA. Also discuss one marketing
authorization procedure in EU. (15)
Q5. Explain the following is relation of Hatch Waxman act. (5?3)
a) 30 month stay
b) NCE exclusivity
c) Discuss the import of cosmetic in ASEAN countries.
Q6. a) What are the regulatory considerations for manufacturing in Japan? (7.5?2)
b) Write a detailed note on DMF.












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