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Certificate program in clinical research and regulatory affairs from SGS – understand the regulations that you need to observe when performing clinical trials and research in India.

Indian drug registration is governed by a range of regulations. As a result, anyone involved in clinical trials and research must be aware of the regulatory process that applies to the marketing and registration of drugs in India. This course will provide you with an understanding of the regulatory affairs for conducting clinical trials in this country.

Why choose the certificate program in clinical research and regulatory affairs from SGS?

This course will help you:

  • Understand the regulations governing clinical research in India
  • Manage clinical procedures and methods in full compliance
  • Recognise India’s Drugs and Cosmetics Act, and its application to drugs, devices, narcotics and biological stem cell genomic research

The trusted certificate in clinical research and regulatory affairs from India’s leading training provider

As a world leader in certification, verification, inspection and testing for clinical research, we have unrivalled experience in conducting clinical trials for leading pharmaceutical companies across the globe. Plus, as a leading course provider in India, we provide in-depth expertise in training for all aspects of clinical trials.

To find out more about the certificate in clinical research and clinical data management, contact us today.