Primeiro NB designado para o MDR – BSi UK http://ec.europa.eu/growth/tools-databases/nando/index.cfm?fuseaction=directive.notifiedbody&dir_id=34
Posts published in “Medical Device Regulation MDR”
Interesting read from BSI – MDR Documentation Submissions Best Practices Guidelines
MDR and IVDR implementing measures rolling plan – December 2018
Survey regarding where members of Team-nB are in the MDR designation process – Team-NB is publishing a survey on the MDR designation process present stages in…
Manufacturers with CE Marking shall update their procedures and forms. Fabricantes com Marcação CE devem atualizar seus procedimentos e formulários. Manufacturer Incident Report (MIR) for Serious…