What are common mistakes and tips how properly draw up the Technical documentation (TD) for medical device?
Recently the NB Team (The European Association of Medical devices Notified Bodies) endorsed the document which can be consider as up-to-date guidance for creating or updating the TD. The document called "Best Practice Guidance for the Submission of Technical Documentation under Annex II and III of Medical Device Regulation (EU) 2017/745" contains common guidance on what is important to submit in TD. As is written through Notified bodies it can be also consider what is expected in order to submit proper TD for the medical devices.
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