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Regulation 745/2017 on Medical Devices: post market activities and follow up

September 29 @ 10:30 am - 12:30 pm
Regulation 745/2017 on Medical Devices: technical file structure

October 13 @ 10:00 am - 12:30 pm
Regulation 745/2017 on Medical Devices: Unique Device Identification number requirements

October 27 @ 10:00 am - 12:00 pm

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Biological Safety Evaluation ISO 10993 – Risk Approach – In Vivo – In Vitro Test – Technical File – Live Webinar
Live Webinar – Regulation 745/2017 on Medical Devices – 5 Lessons – 8 Hours
How FDA Trains Its Investigators to Review CAPA, and Best Practices for Preparation
Complaint Handling in Compliance with FDA and ISO Regulations – 1,5 hours webinar
Live Webinar Clinical Evaluation and literature data according to MEDDEV 2.7.1 rev June 2016 – May 29
Live Webinar (UDI) Unique Device Identification according to New Medical Devices Regulation – 26 April

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