Rajiv Gandhi University of Health Sciences, Karnataka
V Year Pharm-D (II Year Pharm D Post Baccalaureate) / V Year Pharm-D Degree Examination – 04-Jan-2020
Time: Three Hours Max. Marks: 70 Marks
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CLINICAL RESEARCH
Q.P. CODE: 2874 / 2890
Your answers should be specific to the questions asked. Draw neat, labeled diagrams wherever necessary.
LONG ESSAYS (Answer any two) 2 x 10 = 20 Marks
- Explain the different post marketing surveillance methods and explain them.
- Explain the ethical guidelines for clinical research.
- Describe the various drug characterization techniques during drug development process.
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SHORT ESSAYS (Answer any six) 6 x 5 = 30 Marks
- Explain the toxicological approach in drug discovery.
- Describe the role of clinical research associate.
- Explain the components of data management.
- Describe pre-clinical trials.
- Explain about elements of informed consent process.
- Explain about composition and responsibilities of institutional review board.
- Explain the role of sponsor.
- Describe about the regulatory system in Europe
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SHORT ANSWERS 10 x 2 = 20 Marks
- List the critical pharmacokinetic parameters in drug development.
- Define human equivalent dose.
- Define confidentiality.
- Define case control studies.
- List the different types of blinding.
- Methods to take informed consent in research involving children.
- Write any two challenges in the implementation of guidelines.
- Define regulatory authority.
- Define abbreviated new drug application.
- Explain the importance of drug master file.
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