PG Diploma in Regulatory Affairs

Programme Overview

The Postgraduate Diploma in Regulatory Affairs PGDRA at MIT-WPU is tailored to offer advanced education and training in regulatory sciences with a British English emphasis. The programme aims to equip students with the knowledge and skills necessary to address the challenges of an ever-evolving global environment. It places a significant focus on ensuring the safety and efficacy of diverse products, including pharmaceuticals, biopharmaceuticals, veterinary medicines, medical devices, pesticides, agrochemicals, cosmetics, and complementary medicines. Employing a multidisciplinary approach that amalgamates concepts, tools, and techniques from various fields, the PGDRA programme trains students to uphold public health standards by meeting regulatory requirements at the local, regional, and global levels throughout the entire drug development and commercialisation process. The curriculum comprehensively covers all facets of drug development, approval, and marketing, providing students with a thorough understanding of the regulatory landscape governing these processes. This programme is particularly advantageous for working professionals seeking to enhance their skills in the regulatory affairs sector, offering them an excellent opportunity to upskill and stay abreast of industry specific requirements.

1 Year

Last Date To Apply : 17 May 2024
Programme Name

PG Diploma in Regulatory Affairs

Fee Per Year


Highest CTC


Minimum 50% aggregate score in any stream of graduation (3/4-years) or equivalent from Govt. Approved University Life Sciences as a subject in graduation & should be a working professional.

Selection Process

The selection process for the programme is based on MIT-WPU CET PI (Personal Interaction) 2024 score.

Programme Highlights
  • Unique program for the working professionals.
  • Industry oriented curriculum.
  • Guidance by the industry experts
  • Hands on training for ECTD software
Career Prospects
  • Drug Regulators
  • Manufacturing Operations: Pharmaceuticals and Biologicals
  • Regulatory submissions: Medical Devices, Pharmaceuticals and Biologicals
  • Regulatory Consultants
  • Regulatory Affairs Officers
  • Scientific Writers
  • Regulatory Affairs Technical
  • Pharmacy Legal Consultants
Placements & Recruiters
100% placement assistance
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