Compliance with the new Medical Device Regulation.
Our client wished to review one of its product’s Technical File against the new Medical Device Regulation (EU 2017/745) to identify what changes would needed to be made and /or additional information included to bring it into compliance with the new Regulation. We performed a gap analysis and made the appropriate recommendations to the client.
We are a specialist medical device consultancy consisting of industry experts with long and successful track records in commercialising medical device products. We have broad functional and sector experience, and would welcome an opportunity to discuss with you any challenge relating to creating sustainable value from medical technologies.
Munna Choudhury of Alacramed will be attending UK BIOTECH SUMMIT 2019, on
Mark Wickham of Alacramed will be attending Med-Tech Innovation Expo 2019 at
We understand the need for accurate, tailored health economic and budget impact
Alacramed Ltd, St Johns Innovation Centre, Cowley Road, Cambridge,
+44 (0) 1223 421885