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.

Pursuing Regulatory Affairs at SVCP is a rewarding, intellectually stimulating and highly regarded by Industries.

• The autonomous status of the institution facilitated refining of the curriculum to meet the current industry needs with the joint exercise of industry and academia experts
• Highly qualified and experienced faculty from academics and industry
• Practicing best learning strategies for understanding various countries regulations with number of brainstorming case study discussions  with visiting industry experts
• Track record of 100% placements in more than 20 companies
• Regulatory Affairs Graduates from SVCP having acquired allied knowledge in areas of Quality Assurance, Clinical Affairs, Project Management, and Marketing would enable them to work in other related fields.