top of page
CE Marking & FDA Regulations Workshop
Thu 13 Feb
|Webex
SEHTA and Psephos Biomedica are running their next workshop on CE Marking & FDA Regulations requirements.
Registration is Closed
See other events
Time & Location
13 Feb 2020, 14:00 GMT
Webex
About the event
SEHTA and Psephos Biomedica are running their next workshop on CE Marking & FDA Regulations requirements.
Medical technology developers are faced with choices on which markets to access first. The EU and the US represent 2/3 of all spend on medical devices and so understanding what is required to access these two markets is essential.
This one day interactive workshop will provide an overview of:
CE Marking
MDR CE Marking Process and the role of a Notified Body and Competent
AuthorityMDR Device Classification
bottom of page