Technical Management to bring a medical device to a standard that is capable of being certified, manufactured, distributed and supported
Development and support of the Risk Management File,
required to bring the medical device to market
Management of the process to obtain compliance to the Medical Device Safety Standard ISO 60601
Development of the Technical File and assistance with the submission to the Notified Body to obtain the CE mark for the Medical Device
+44 (0) 7801 017 892