Medilink

With the continued development and integration of software in medical device applications it can be difficult to understand the complex structure surrounding product classification and the implications this has for CE marking and ISO accreditation.

This interactive workshop run by David Warwick, Head of Software and Regulatory Affairs at EG Technology will focus on how to design medical device software for regulatory approval.

Covering the practical application of ISO 62304 and how this integrates with other regulatory aspects of medical device approval, this workshop will allow you to openly discuss the accreditation process and use peer-to-peer discussions to find solutions.

Places are free of charge for Medilink Y&H member companies and are charged at £40 for non-members.

To book your place, please click here.