Industry Program In Pharma Regulatory Affairs

Course Overview

The efficacy of a drug varies with the age, body weight, immunity state etc. Thus no drug is completely safe or harmful. However, it is legally as well as morally expected to take appropriate steps should be taken by the producing company to ensure optimal quality, safety and efficacy of the drug. A regulatory affair professional ensures the regulatory compliance in the company and prepares submissions documents for the drugs with the appropriate authorities. This department has to keep pace with the new development in the scientific as well as regulatory rules issuing departments at national and international level. Thus this department is least perturbed by mergers and acquisition and also during recession. Continual education is however, necessary to these professionals.

Career Opportunities

The program equips students with the understanding of the regulatory processes involved in biotechnology, medical device, pharmaceutical and food products at national and international level. This specialized knowledge enables regulatory affair professionals to help biotechnology, medical device, pharmaceutical and food companies manage regulatory processes. The students after completion of the course work as

  • Pharma Regulatory Affairs Consultant
  • Regulatory Officer

Course Objectives

The industry program aims to prepare aspirants for regulatory affairs positions in the pharmaceutical, biopharmaceutical and medical device industries and equip them with the educational foundation that will help them advance in the regulatory affairs profession. This program is intended to provide students with a basic understanding of the areas of regulatory affairs and quality operations. It give students a thorough and up-to-date knowledge of federal laws and regulations and their application at various stages of the development and commercialization of pharmaceutical, biopharmaceutical and medical device products. The legal and regulatory issues are very critical to Pharma companies, Clinical Research Organization and Bio Tech companies. The course focuses on regulatory affairs concept which these organizations must comply to sell their products both domestically and at the international market.

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