Exam Details
Subject | advanced pharmaceutical analysis | |
Paper | ||
Exam / Course | m.pharm | |
Department | ||
Organization | G. Pulla Reddy College Of Pharmacy | |
Position | ||
Exam Date | February, 2018 | |
City, State | telangana, hyderabad |
Question Paper
FACULTY OF PHARMACY
M. Pharmacy (Pharma. Analysis) I-Semester (Main) Examination, February 2018
Subject: Advanced Pharmaceutical Analysis
Time: 3 Hours Max. Marks: 75
Note: Answer any five questions. All questions carry equal marks.
1 Explain in-detail about impurity profiling of new drug product.
Write classification and identification of elemental impurities.
2 Explain briefly protocol adopted for stability testing of drugs.
Describe briefly accelerated stability studies and determination of shelf-life.
3 Explain various principles and testing procedures involved in degradant
characterization.
Describe ICH stability guidelines for biological products.
4 Write an account on requirements for stability testing of phytopharmaceuticals.
Describe the principle and methods involved in HPLC finger printing with
suitable examples.
5 Mention different types of tetanus vaccine. Explain bioassay of adsorbed
tetanus vaccine.
Describe the principle and procedure involved in bioassay of any one biological
product.
6 Describe the principle, instrumentation and applications of radio immune assay.
Describe procedures for separation of bound and unbound drug during
immunoassay.
7 Write an account on elemental impurities and their determination.
Explain basic principle and applications of PCR studies.
8 Write classification, potential sources, control and identification of residual solvent
impurities.
Describe the production of antibodies.
M. Pharmacy (Pharma. Analysis) I-Semester (Main) Examination, February 2018
Subject: Advanced Pharmaceutical Analysis
Time: 3 Hours Max. Marks: 75
Note: Answer any five questions. All questions carry equal marks.
1 Explain in-detail about impurity profiling of new drug product.
Write classification and identification of elemental impurities.
2 Explain briefly protocol adopted for stability testing of drugs.
Describe briefly accelerated stability studies and determination of shelf-life.
3 Explain various principles and testing procedures involved in degradant
characterization.
Describe ICH stability guidelines for biological products.
4 Write an account on requirements for stability testing of phytopharmaceuticals.
Describe the principle and methods involved in HPLC finger printing with
suitable examples.
5 Mention different types of tetanus vaccine. Explain bioassay of adsorbed
tetanus vaccine.
Describe the principle and procedure involved in bioassay of any one biological
product.
6 Describe the principle, instrumentation and applications of radio immune assay.
Describe procedures for separation of bound and unbound drug during
immunoassay.
7 Write an account on elemental impurities and their determination.
Explain basic principle and applications of PCR studies.
8 Write classification, potential sources, control and identification of residual solvent
impurities.
Describe the production of antibodies.
Other Question Papers
Subjects
- advanced pharmaceutical analysis
- food analysis
- modern pharmaceutical analytical techniques
- pharmaceutical validation