Regulation of COVID-19 Tests in the EU: when do you need to involve a Notified Body?

Published date22 October 2020
Subject MatterMedical Devices,EU,Regulatory Agenda,Diagnostic Tests,EU Directive,Public Health,Infectious Diseases,Pharmaceutical Industry,Coronavirus/COVID-19,Virus Testing,AFMPS
AuthorFabien Roy,Hélène Boland
Law FirmHogan Lovells

To continue reading

Request your trial

VLEX uses login cookies to provide you with a better browsing experience. If you click on 'Accept' or continue browsing this site we consider that you accept our cookie policy. ACCEPT