 |
The following checklist gives an overview of the required documents essential as per MDR for a precise implementation of the clinical product lifecycle. |
|
Since now the medical device coordination group (MDCG) has published some new guidelines on how to implement the MDR (EU) 2017/745 more specifically pertaining to clinical investigation and clinical evaluation. And it is already an established fact that the documents and records required by the MDR is much more extensive than … |
||
CERES
Your Professional CRO-Team for Medical Devices
