This afternoon event will focus on the requirements for Technical Documentation under the MDR/IVDR and the practical implementation thereof. It will feature expert speakers and designated time for an interactive Q&A session.Scheduled presentations include:Technical Documentation Under MDR/IVDR Dr. Itoro Udofia, Head of Notified Body, UL International
Legacy Products: Steps to Get Technical Documentation Ready for Conformity Assessment Under MDR/IVDRPhilippe Etter, Medidee Services
UDI - Status and Practical ApproachRoland Weibel, GS1 System Switzerland
Regulatory Affairs Professionals Society (RAPS)5635 Fishers Lane, Suite 400Rockville, Maryland 20852
raps@raps.org+1 301 770 2920
JoinMy RAPS DashboardLearn More
About UsTerms of UsePrivacy Policy