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This intensive course enables you to gain a detailed understanding of the clinical evaluation process for medical devices against the requirements of the Medical Device Regulation (MDR - EU 2017/745), MEDDEV 2.7/1 Revision 4 and relevant MDCG guidance documents.
The course will help you:
On completion of this training, you’ll be able to:
Clinical and Regulatory Affairs Professionals, Medical Device R&D Engineers and Scientists.
On completion, you’ll be awarded an internationally recognized BSI Training Academy certificate.
If you have any enquiries, let us know how can we help you.
Call: +91 80815 80815
Email us: info.in@bsigroup.com
Please Note: This training fee is applicable only for residents of India and the Indian subcontinent.
Reach out and see how we can help guide you on your path to sustainable operational success.