Do you want to Learn about EU MDR (European Medical Device Regulation)?
We Provide training courses on (EU-MDR/2017/745 & CE marking) with recorded lectures,
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This course will help you to understand:
The MDR’s additional requirements
The current directives – MDD 93/42/EE and ISO 13485:2016
Terminology and certification requirements
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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
