EU MDR 2017/745 Medical Devices General Safety and Performance Requirements

In this webinar, you will how to manage General Safety and Performance Requirements (GSPRs) according to EU MDR 2017/745 Annex I for full compliance with new EU Medical Device Regulation mandatory starting 26-May-2021

Why Should You Attend:

New EU MDR 2017/745 will be mandatory starting 26-May-2021. General Safety and Performance Requirements (GSPRs) are one of the specific areas where MDR has introduced new requirements versus previous EU Medical Device Directive MDD 93/42/EEC. It is key for all medical device manufacturers to ensure compliance with new EU MDR (that will allow EU market commercial activity).

Areas Covered in the Webinar:

• Required rationale
• Matrix
• MDR GSPRs vs MDD ERs
• New approach

Who Will Benefit:

Medical device industry Regulatory Affairs,

Regulatory Compliance and Quality Assurance Managers,

Directors and VPs.