Exam Details
| Subject | modern pharmaceutical analysis | |
| Paper | ||
| Exam / Course | m.pharm | |
| Department | ||
| Organization | Gujarat Technological University | |
| Position | ||
| Exam Date | May, 2017 | |
| City, State | gujarat, ahmedabad |
Question Paper
Seat No.: Enrolment
GUJARAT TECHNOLOGICAL UNIVERSITY
M. Pharm SEMESTER II • EXAMINATION SUMMER 2017
Subject code: 1921501 Date: 29/05/2017
Subject Name: Modern Pharmaceutical Analysis
Time: 10:30 AM to 01:30 PM Total Marks: 80
Instructions:
1. Attempt any five questions.
2. Make suitable assumptions wherever necessary.
3. Figures to the right indicate full marks.
Q.1
Define cosmetic. Discuss evaluation of cosmetic products in detail.
08
Write note on automated analysis.
08
Q.2
State the importance of solid-state analysis. Explain solid state analysis at particulate level with suitable examples.
08
Explain IPQC test for solid oral dosage form.
08
Q.3
Briefly explain Isoelectric focusing technique.
06
Explain Tryptic mapping technique in detail.
05
Explain in detail Amino Acid Sequence Analysis.
05
Q.4
What is the importance of regulatory guidelines in pharmaceutical analysis? Explain US-FDA guidelines in brief.
08
Enlist the quality control tests for medicinal plant material as per WHO. Describe any four in brief.
08
Q.5
Enlist different analytical tests for finished parenteral products. Write note on sterility testing.
08
What is pre-formulation study Explain the importance of pre-formulation studies . Describe the analytical techniques for pre-formulation studies.
08
Q. 6
Describe in detail solid state analysis of pharmaceuticals at molecular level.
06
What is polymorphism? Explain its significance in formulation development.
05
What is impurity? Classify the impurities encountered in pharmaceuticals. Discuss organic impurities obtained from synthetic process.
05
Q. 7
Explain compendial testing of active pharmaceutical ingredient with example.
06
Discuss ICH guidelines laid down for stability studies of pharmaceuticals
05
Discuss quality control of radiopharmaceuticals.
05
GUJARAT TECHNOLOGICAL UNIVERSITY
M. Pharm SEMESTER II • EXAMINATION SUMMER 2017
Subject code: 1921501 Date: 29/05/2017
Subject Name: Modern Pharmaceutical Analysis
Time: 10:30 AM to 01:30 PM Total Marks: 80
Instructions:
1. Attempt any five questions.
2. Make suitable assumptions wherever necessary.
3. Figures to the right indicate full marks.
Q.1
Define cosmetic. Discuss evaluation of cosmetic products in detail.
08
Write note on automated analysis.
08
Q.2
State the importance of solid-state analysis. Explain solid state analysis at particulate level with suitable examples.
08
Explain IPQC test for solid oral dosage form.
08
Q.3
Briefly explain Isoelectric focusing technique.
06
Explain Tryptic mapping technique in detail.
05
Explain in detail Amino Acid Sequence Analysis.
05
Q.4
What is the importance of regulatory guidelines in pharmaceutical analysis? Explain US-FDA guidelines in brief.
08
Enlist the quality control tests for medicinal plant material as per WHO. Describe any four in brief.
08
Q.5
Enlist different analytical tests for finished parenteral products. Write note on sterility testing.
08
What is pre-formulation study Explain the importance of pre-formulation studies . Describe the analytical techniques for pre-formulation studies.
08
Q. 6
Describe in detail solid state analysis of pharmaceuticals at molecular level.
06
What is polymorphism? Explain its significance in formulation development.
05
What is impurity? Classify the impurities encountered in pharmaceuticals. Discuss organic impurities obtained from synthetic process.
05
Q. 7
Explain compendial testing of active pharmaceutical ingredient with example.
06
Discuss ICH guidelines laid down for stability studies of pharmaceuticals
05
Discuss quality control of radiopharmaceuticals.
05
Other Question Papers
Subjects
- advanced medicinal chemistry
- advanced organic chemistry-i
- advanced organic chemistry-ii
- advanced pharmacology ii
- advanced pharmacology-i
- advances in drug delivery system
- advances in pharmacology
- applied pharmacotherapeutics - ii
- applied pharmacotherapeutics-i
- audits and regulatory compliance
- biological evaluations & clinical research
- cellular and molecular pharmacology
- clinical and hospital pharmacy
- clinical pharmacy practice
- clinical research and pharmacy practice
- clinical research and regulatory affairs
- clinical research regulations
- cosmetic and cosmeceuticals
- documentation and regulatory writing
- drug design and discovery
- drug regulation and regulatory authority
- experimental design and patents
- global regulatory requirements
- gmp, glp and validation
- good manufacturing and good laboratory practice
- good manufacturing practice and process validation
- good regulatory practices
- hazards and safety management
- industrial pharmacy practice
- modern analytical techniques
- modern pharmaceutical analysis
- novel drug delivery system part-i
- novel drug delivery system-ii
- pharm. management -ii
- pharmaceutical analysis ii
- pharmaceutical and cosmetic analysis
- pharmaceutical formulation and development
- pharmaceutical formulation development and biopharmceutics
- pharmaceutical manufacturing technology
- pharmaceutical production management & technology
- pharmaceutical regulatory affairs
- pharmacological and toxicological screening methods-i
- pharmacological and toxicological screening methods-ii
- pharmacometrics and methods of biological evaluation of drugs
- pharmacotherapeutics
- principles of biopharmaceutics& pharmacokinetics
- product development and technology transfer
- quality control & quality assurance
- quality control and quality assurance
- quality management system
- regulatory affairs - i
- regulatory affairs and new drug applications
- regulatory aspects of hebbal and biologicals
- research methodology
- validation and product development