Exam Details

Subject clinical pharmacy practice
Paper
Exam / Course m.pharm
Department
Organization Gujarat Technological University
Position
Exam Date May, 2017
City, State gujarat, ahmedabad


Question Paper

Seat No.: Enrolment No.
GUJARAT TECHNOLOGICAL UNIVERSITY
M. Pharm SEMESTER-I • EXAMINATION SUMMER-2017
Subject Code: 910106 Date: 29/04/2017
Subject Name: Clinical Pharmacy Practice
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 Explain role of clinical pharmacists in a tertiary care hospital.
Mention the contribution of Pharmacist in ward rounds.
Write short note on Pharmaceutical care concept.
Q.2 Write a short essay on Essential drug list. Write a short note on OTC drugs, AND
Rational prescribing.
Q.3 Write a short essay on ADR monitoring. How ADR monitoring differs from Drug therapy monitoring.
Write short note on medication errors.
Q.4 Define Pharmacoeconomics explain the needs of pharmacoeconomic studies.
Write short notes on cost effectiveness evaluation, AND
Cost benefit evaluation.
Q.5 What are the various types of Drug interaction? Explain with example.
Mention the methods for minimizing clinically relevant drug interaction.
Explain the role of pharmacist in monitoring the same.
Q.6 Write an essay on quality assurance of pharmacy serious. Mention the various tests associated with liver function, AND Thyroid function tests.
Q.7 Write a short essay on Drug utilization studies.
Mention the contribution of Drug utilization studies in clinical practice.
Write short note on patient compliance.



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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