Exam Details
Subject | pharmaceutical jurisprudence | |
Paper | ||
Exam / Course | pharm d (6–ydc) | |
Department | ||
Organization | G. Pulla Reddy College Of Pharmacy | |
Position | ||
Exam Date | July, 2018 | |
City, State | telangana, hyderabad |
Question Paper
FACULTY OF PHARMACY
Pharm D III Year (Main Backlog) Examination, July 2018
Subject: Pharmaceutical Jurisprudence
Time: 3 Hours Max.Marks: 70
Note: Answer all questions from Part A. Any Five questions from Part B.
PART A (10x2 20 Marks)
1 Define V P Schedules according to D C Act.
2 Give the cautionary labeling requirement for Schedules H drugs.
3 Do all the OTC medications are prescribed drugs. Justify.
4 Distinguish between misbranded and adulterated drug.
5 What is repacking license?
6 In which two central govt. factories opium can be manufactured?
7 What is the differentiation between 'Pharmacy' and 'Chemist Druggist
8 Define 'Design' under Design Act.
9 What are different types of IPR?
10 What is legal definition of 'Cosmetics'?
PART B (50 Marks)
11 Write a note on Schedule Y.
12 What are the power and duties of drug inspector?
13 Classify the drugs according to prescribe and non-prescribe drugs.
14 Write about first, second and third schedule of Drug Price Control order and mention
the formula for calculation of retail price.
15 Describe the objectives of drugs enquiry committee 1930.
16 What is patent? Write the procedure for getting patent.
17 Enlist the prohibition of advertisement and penalties as per Drugs and Magic
Remedies Act.
18 Write down in brief about the code of Pharmaceutical Ethics.
Pharm D III Year (Main Backlog) Examination, July 2018
Subject: Pharmaceutical Jurisprudence
Time: 3 Hours Max.Marks: 70
Note: Answer all questions from Part A. Any Five questions from Part B.
PART A (10x2 20 Marks)
1 Define V P Schedules according to D C Act.
2 Give the cautionary labeling requirement for Schedules H drugs.
3 Do all the OTC medications are prescribed drugs. Justify.
4 Distinguish between misbranded and adulterated drug.
5 What is repacking license?
6 In which two central govt. factories opium can be manufactured?
7 What is the differentiation between 'Pharmacy' and 'Chemist Druggist
8 Define 'Design' under Design Act.
9 What are different types of IPR?
10 What is legal definition of 'Cosmetics'?
PART B (50 Marks)
11 Write a note on Schedule Y.
12 What are the power and duties of drug inspector?
13 Classify the drugs according to prescribe and non-prescribe drugs.
14 Write about first, second and third schedule of Drug Price Control order and mention
the formula for calculation of retail price.
15 Describe the objectives of drugs enquiry committee 1930.
16 What is patent? Write the procedure for getting patent.
17 Enlist the prohibition of advertisement and penalties as per Drugs and Magic
Remedies Act.
18 Write down in brief about the code of Pharmaceutical Ethics.
Other Question Papers
Subjects
- biology
- biopharmaceutics & pharmacokinetics
- biostatistics & research methodology
- clinical & pharmacokinetics pharmacotherapeutic drug monitoring
- clinical pharmacokinetics and pharmacotherapeutic drug monitoring
- clinical pharmacy
- clinical research
- clinical toxicology
- community pharmacy
- hospital pharmacy
- human anatomy and physiology
- medicinal biochemistry
- medicinal chemistry
- pathophysiology
- pharmaceutical analysis
- pharmaceutical formulations
- pharmaceutical inorganic chemistry
- pharmaceutical jurisprudence
- pharmaceutical microbiology
- pharmaceutical organic chemistry
- pharmaceutics
- pharmacoepidmiology and pharmacoeconomics
- pharmacognosy & phytopharmaceuticals
- pharmacology – i
- pharmacology – ii
- pharmacotherapeutics – i
- pharmacotherapeutics – iii
- pharmacotherapeutics-ii