The objective of Post Graduate Diploma in Drug Regulatory Affairs program is to develop students, over the period of 6 months, by in depth industry oriented knowledge to reach top end positions in the pharmaceutical regulatory affairs industries.
This program is developed and structured in a manner to match high academic standards and international regulatory industry requirements. The comprehensive syllabus of ICH Quality guidelines, eCTD submission, API and Formulation regulatory submission to developed and developing market along with workshop on Interview techniques, CV development ensure a fast successful corporate career.
- Classroom Lectures
- Assignments/ Project
6 Months- Every Sunday.