We provide consultation for Medical and In-vitro Medical Device CE, US FDA, NIOSH, ISO, and Indian MDR certification along with services like Appointment of Authorized Representative, External testing services, EUDAMED registration, UDI Labelling, Registration on Sugam portal, Conformity assessment, Document review, and Audit NC closures. Our training & consulting support helps medical device customers to design & manufacture their products in compliance with regulatory requirements and bring them to the market more quickly, effectively & efficiently.

https://mavenprofserv.com/