Exam Details

Subject research methodology
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-II • EXAMINATION SUMMER 2017
Subject Code: 2920001 Date: 26/05/2017
Subject Name: RESEARCH METHODOLOGY
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

What is mean by research? What are the objectives of research?
06

What are the different types of research? Explain any one in detail.
05

What is literature review? What are the sources for literature review?
05
Q.2

Write a note on PSAR.
06

Write a brief note on different types of analysis of data. pointing out the significance of each in research.
05

Which are the limitations and sources of errors in research?
05
Q.3

How will you prepare research proposal for procurement of research grant. Explain in detail.
06

Write in detail on documentation techniques in research.
05

What is the importance of documentation in research?
05
Q.4

Discuss different parts of thesis.Disucss any two in detail.
06

What are the qualitative tools in Research?
05

Give importance of research paper writing. Describe various sections of research paper writing.
05
Q.5

Enlist the important factors for successful oral presentation. Discuss any two in detail.
06

Discuss art of preparing good poster presentation.
05

Describe types, characteristics and functions of hypothesis.
05
Q. 6

How can one analyze the cost requirements for a project? Describe it.
06

Explain the methods used for literature survey on the internet.
05

List out the International, Government and Private agencies for research grants.
05
Q.7

Describe the importance of IIIC. Explain the activities of IIIC.
06

Write a note on feasibility reports.
05

Write a note on characteristics of good questionnaire.
05



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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