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.

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.