paper
The following checklist gives an overview of the required documents essential as per MDR necessary for a precise implementation of the clinical product lifecycle.

 

 
Further questions?
Talk with our experts, or use our contact form:

Contact  

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 …
Read more