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.
Our consultant Munna Choudhury will be leading a Round Table discussion on
Our consultant Munna Choudhury attended the FierceBiotech Executive Summit in London on
Munna Choudhury of Alacramed will be attending the Fierce Biotech UK Summit on
Alacramed Ltd, St Johns Innovation Centre, Cowley Road, Cambridge,
+44 (0) 1223 421885