To make available a pool of competent professionals in the area of Pharmaceutical Regulatory Affairs with fundamental knowledge on
- Various Good Regulatory Practices in the Healthcare and related industries.
- Documentation and general principles involved in regulatory writing and submission to agencies.
- Audit, inspections, Quality management system and Product Life Cycle Management.
- Clinical drug development and research regulations in India, EU and US
- Regulations for Drugs, Cosmetics, Medical Devices, Herbals, Biologics, Food and Nutraceuticals in various countries like India, EU, US, Canada, Japan, ASEAN, etc