Training Program on European Medical Device Regulation,
Do you want to Learn EU MDR (European Medical Device Regulation)?
We Provide training course on (EU-MDR/2017/745 & CE marking) with recorded lectures,
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WHAT IS EUMDR?
Implementation of European Medical Device Regulations is the primary requirement while demonstrating the compliance to regulatory requirements while placing the products in European Market for the Medical Device manufacturers and to place CE marking on the products.
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WHO SHOULD ATTEND?
Manufacturers of medical devices, especially: Regulatory Affairs, Design and Development, Clinical Affairs Specialists, Quality Management, and Quality Assurance personnel.
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Hurry Up,
Register now at GIRA ,
CALL/WHATSAPP For Enquiry:
+91-9595750750
More info visit:http://bit.ly/3sZQbEc
