What: Webinar – “Implementing and Maintaining PMS and Performance Evaluation under the IVDR”
When: Thursday, September 29th, 2022, at 10 am CT
Where: Online Event
How: Register Here
Why: This webinar will illustrate how the PMS process interoperates with other systems including Performance Evaluation, Risk Management and Post Market Performance Follow-Up to continuously update key elements of the Technical Documentation.
The EU In Vitro Diagnostic Devices Regulation (IVDR) brings together previously disparate components of the quality system and requires them to interoperate in a highly synchronous manner with Post Market Surveillance (PMS) driving the documentation cycle for each product in a manufacturer’s portfolio.
This featured presentation will be led by Celegence’s Regulatory Affairs Subject Matter Expert for Medical Devices and IVDs James Shearn. James will also be available following the presentation for a live Q/A session.
Celegence will be hosting the WEBINAR on Thursday, September 29th at 10 am CT.Register online now!