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PG Diploma in Drug Regulatory Affairs

PGDDRA (PG Diploma in Drug Regulatory Affairs )

The pharmaceutical, biotechnology and medical device research and development industries are among the most
highly regulated industries globally. As pharmaceutical sector is growing rapidly, there is a need of regulatory
affairs professionals to cater the current needs of industries for the global competition. Regulatory affairs
professionals are the link between pharmaceutical industries and worldwide regulatory agencies. Pharmaceutical
Industry, being one of the highly regulated industries, is in immense need of people than ever before who are
capable of handling issues related to regulatory affairs in a comprehensive manner.

Program Codebest PGDDRAPGDDRA
Duration Min. Duration1 Years
Max. Duration3 Years
Eligibility CriteriaGraduate in Science Stream

 

 

 

Tution Fees per annum 12,000/-

YEAR I

Course Code

Course Title

Theory/Practical

Continuous Assessment (Internals)

Credits

DRA15101Pharmaceutical Practices and Regulation.

70

30

8

DRA15102Quality Assurance,GMPand Regulation.

70

30

8

DRA15103Drug Regulatory Affairs including International Aspects.

70

30

8

PRJ15101Project

200

4

Total

28

Please click here to download a copy of the syllabus

After the completion of PGDDRA, you will find a challenging career in a hospital and healthcare industry

Common job profiles of students after completing PGDDRA include:

Medical and Health Services Managers, Hospital Administrator, Manager, Senior Manager, Hospitals and other Senior Leadership Positions.

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