Regulatory affairs is comparatively a new profession which was developed by the government to protect public health by controlling the safety and efficacy of products in areas including pharmaceuticals, veterinary medicines, medical devices, pesticides, agrochemicals, cosmetics and complementary medicines.
This program is designed to impart fundamental knowledge on various Good Regulatory Practices viz., cGMP, GLP, GALP and GDP for Pharmaceuticals, Cosmetics, Food & Nutraceuticals, Medical devices etc.
Regulatory Affairs professionals coordinate and document internal regulatory processes, such as internal audits, inspections, license renewals, or registrations. Regulatory Affairs plays a crucial role in the pharmaceutical industry and is involved in all stages of drug discovery, development, marketing approval and post marketing surveillance.