2019-08

The Regulation (EU) 2017/745 on medical devices requires that the manufacturer shall draw up a summary of safety and clinical performance (SSCP) for implantable devices and for class III devices, other than custom-made or investigational devices. The SSCP shall be validated by a notified body (NB) and made available to the public via the European database on medical devices (Eudamed)

The main purpose of this document (MDCG 2019-9) is to provide guidance on the presentation, content and validation of the SSCP.

The guidance can be downloaded in our library

Source: https://ec.europa.eu/growth/sectors/medical-devices/new-regulations/guidance_en