Jun 13, 2022
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, . . 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 . . WHO SHOULD ATTEND? Manufacturers of medical devices, especially: Regulatory Affairs, Design and Development, Clinical Affairs Specialists, Quality Management, and Quality Assurance personnel. . . Hurry Up, Register now at GIRA, CALL/WHATSAPP For Enquiry: +91-9595750750 More info visit:http://bit.ly/3sZQbEc