Blog Article: What does the MDR tell us about post-market surveillance? -- MEDICA - World Forum for Medicine

11/01/2018

Castor EDC

Blog Article: What does the MDR tell us about post-market surveillance?

With the Medical Device Regulation (MDR) coming into full force in 2020, medical device companies should prepare for tougher Post-Market Surveillance (PMS) requirements. Companies will need to update their PMS procedures and should budget for more Post-Market Clinical Follow-up (PMCF) studies.

This article will address the role of Post-Market Surveillance during the lifecycle of your device, the specific requirements for Post-Market Surveillance under the MDR, and how an EDC system can help you fulfill these requirements in a cost-effective way. We will cover:

1) the role of Post-Market Surveillance during the lifecycle of your device;

2) the specific requirements for Post-Market Surveillance under the MDR;

3) how an Electronic Data Capture (EDC) system can help you fulfill these requirements in a cost-effective way.

Download your copy of the White Paper from the link below

Exhibitor Data Sheet