Sponsored: Post-Market Surveillance requirements

Sponsored: Post-Market Surveillance requirements
FREE SPONSORED WEBINAR - Post-Market Surveillance requirements for Medical Devices and IVDs
Date:  6 December 2022
Time: 15:00 - 16.00 GMT

This webinar will focus on the regulatory requirements for post-market surveillance (PMS) under the European Medical Device Regulations 2017/745 (MDR) and In Vitro Diagnostic medical device Regulations 2017/746 (IVDR). In this 60 minute webinar QBD will explain how PMS includes all the activities carried out by the manufacturer to monitor, measure and assess the device’s quality, performance and safety to ensure that the benefit-risk profile of the device remains current. QBD will also briefly dive into the concept of Post Market Clinical Performance Follow-up (PMCF) for medical devices and Post-Market Performance Follow-up (PMPF) for IVDs. 

Learning Objectives:
Understanding the PMS requirements imposed by the MDR and IVDR, as well as gaining a basic understanding of PMPF and PMCF. After the webinar you will know what needs to be created in terms of plans and reports.

Audience
PMS is a cross-functional activity, therefore this webinar can be of interest to anyone with an IVD or Medical Device manufacturer organisation that will be involved in gathering PMS related information.

This webinar is sponsored by QBD Group.



Disclaimer
Whilst TOPRA is running this webinar for QBD Group, this is not an endorsement of QBD Group, QBD Group's affiliates, employees or its products and services. TOPRA is also not responsible for the content or views expressed during the webinar.

 
When
06/12/2022 15:00 - 16:00
Where
ONLINE
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