Mission : To make the JSS College of Pharmacy Ooty a preferred destination to study Pharmaceutical Regulatory Affairs.

Vission : To make available a pool of competent professionals in the area of Pharmaceutical Regulatory Affairs with fundamental knowledge of various Goof Regulatory Practices in the Health Care and related industry.

Pharmaceutical Regulatory Affairs (PRA) is a vital unit in a pharmaceutical company that successfully drives the Research & Development (R&D) efforts of the company to the market. The regulatory department works with a focus to get products to the market with a commercially viable label, in the least possible time and expense. In view of the increasing global competitiveness among pharmaceutical companies, the key to success lies in obtaining timely marketing approval from the Regulatory agencies of the region where the drug is to be sold. Various government agencies are involved in regulating drugs within their market. The outcome of the program is 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.,

The Objectives of PRA is to prepare professionals for regulatory affairs positions in pharmaceutical sectors, to facilitate the students knowledge with proper foundation in advancing them in the regulatory profession, provide fundamental basics as per industrial requirement in the field of regulatory affairs, keeping track of everchanging legislation in all regions, update students with thorough and up-to-date knowledge of global laws and regulations applicable in various stages of drug development, theoretical and practical knowledge in preparing, compiling and submitting required documents as per industry and regulatory authority needs for the registration of health care products.