Medical device and IVD specialist consultants IMed Consultancy is on hand to discuss how manufacturers can get their devices and IVDs to multiple global markets at Med-Tech Innovation Expo. 

The company covers CE marking under EU Medical Device Regulation (MDR) and In-Vitro Diagnostic Regulation (IVDR), UKCA Marking, IS) 13485 certification and global registrations. 

IMed Consultancy has a team of full time Medical Device and IVD specialist consultants, IMed Consultancy can help manufacturers get their devices and IVDs to multiple global markets. The consultancy works with many start-ups, SMEs and multi-national manufacturers. 

The company is ISO 13485 certified and specialises in Quality Management Systems set up and implementation, as well as internal audit, management review, CAPA and MDSAP. IMed is a registered UK Responsible Person and will shortly be offering an EU Authorised Representative service.

You can find out more by visiting Stand D41. Find out more about Med-Tech Innovation Expo, here. 

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