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 Code | PGDDRA | |
| Duration Min. Duration | 1 Years | |
| Max. Duration | 3 Years | |
| Eligibility Criteria | Graduate in Science Stream |
Tuition Fees per annum 12,000/-
YEAR I
|
Course Code |
Course Title |
Theory/Practical |
Continuous Assessment (Internals) |
Credits |
| DRA15101 | Pharmaceutical Practices and Regulation. |
70 |
30 |
8 |
| DRA15102 | Quality Assurance,GMPand Regulation. |
70 |
30 |
8 |
| DRA15103 | Drug Regulatory Affairs including International Aspects. |
70 |
30 |
8 |
| PRJ15101 | Project |
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.