To be prepared for 26 May 2022, the date of full application of the Regulation Medical Devices – Diagnostics in Vitro, is a real need for professionals and companies, in the field of Regulatory Affairs.

Do not miss the most complete path on the Regulation of Medical Devices – In Vitro Diagnostics: the Specialized Course IVDR (UE) 2017/746 organized by MD24, brand of Thema – a Complife Group Company – dedicated to training.

6 LESSONS X 6 TRAINING DAYS IN LIVE STREAMING!

• Introduction to the Regulation Medical Devices – In Vitro Diagnostics |15 September 2021
• The person responsible for compliance with the Regulation (PRRC) |30 September 2021
• Economic Operators (Representatives, Importers and Distributors) |12 October 2021
• Technical documentation and essential requirements |28 October 2021
• Performance review |11 November 2021
• Post – Market surveillance (PMS) |25 November 2021

PLUS

• Teachers among the best professionals in the sector.
• Theory, simulations, practical exercises, case studies.
• Final certificate demonstrating your skills.
• More than 30% savings compared to the purchase of individual lessons.
• From the 2nd registered persons of the same company: further reduction of -5%.

The course will be held in Italian & in Live Streaming.

Places are limited and registrations close on September 7th. Do not miss this unique opportunity.

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