About the course:

Regulatory Affairs is a comparatively young, multidimensional and growing profession in the Pharmaceutical field with a desire to protect public health. DRA assures safety and efficacy of pharmaceuticals products, veterinary medicines, medical devices, pesticides, agrochemicals, orphan drugs, cosmetics and complementary medicines.

As outsourcing of jobs to India is high, the regulatory affairs industry in India is poised for rapid growth which is associated with flamboyant salaries. There are 120+ pharma companies having structured regulatory affairs department in India. Due to the entry of MNCs in India, it is expected a requirement of 30,000 competent and trained workforce in next 5 years.

If you are looking to start your career in Drug Regulatory Affairs or Pharma Regulatory Affairs or you are already in this industry without any formal training, the course “Certificate Program in Drug Regulatory Affairs” will certify and train you for the entry-level job positions like DRA Executive, Regulatory Affairs Associate.

The course will provide you a comprehensive training on scientific, practical, ethical and technical concepts of the drug regulatory affairs in compliance with regulatory guidelines. This 2 months course covers all the essential topics of DRA in 5 major modules covering 300+ topics. Each module is well explained in detail with the help of illustrations, examples, and flowcharts.

Who Should Enroll?

The course can be attended by:

Health-science professional (working/fresher/ student) from Pharmacy, Life-Science/ Biotech, Medicine, AYUSH (Alternate Medicine), Dental, Nursing, Physiotherapy, Ph.D. background who are looking to gain knowledge & start their career in the pharma or device regulatory domain.

Fresher and experienced regulatory affairs personnel.

How to register:

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