Exam Details

Subject pharm. management -ii
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: 1921602 Date: 31/05/2017
Subject Name: Pharm. Management -II
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

Discuss importance of production planning quality control in product lifecycle.
06

Discuss R D significance in development of quality products.
05

Describe in brief production line job balancing.
05
Q.2

Discuss the role of store keeping inventory management.
08

Describe economic policy, production capacities, manufacturing economics role in production management.
08
Q.3

Describe various motives for sales promotion for maintaining product market demand.
06

Write applications of PERT CPM chart.
05

Discuss factors influencing in selection of plant location.
05
Q.4

Discuss recent advances in packaging for improvement product market demand stability.
06

Describe good warehousing practices its advantages
05

Describe various advance concepts in marketing.
05
Q.5

Discuss product management through corporate management strategy in concern to pharmaceutical industries.
08

Describe various tools techniques for productivity management.
08
Q. 6

Write a detail note on market demand sales forecasting.
10

Discuss in brief: product differentiation addition of product line.
06
Q.7

Write a note on marketing research techniques.
06

Describe non- sterile product layout functional layout with respect to tablets production unit.
05

Write importance of SWOT analysis.
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