EU – State-of-play of joint assessments of Notified Bodies in the medical device sector – June 2019
Posts tagged as “MDR”
Update – MDR and IVDR implementing measures rolling plan
Unique Device Identification (UDI) System – FAQs
EU MDR/IVDR: US Raises ‘Serious Concerns,’ Urges 3-Year Implementation Delay
European implementation of Medical Device and IVD Regulations – Implications for Australia
Single-use medical devices – safety and performance requirements for reprocessing
MHRA guidance updated to reflect the MDR – Clinical investigations of medical devices – Biological safety assessment
BSI – ISO 13485 and products with May 2020 deadline for MDR certification
Application du règlement européen relatif aux dispositifs médicaux : l’ANSM met en place une phase pilote pour la partie investigations cliniques – Point d’information
LA AEMPS COMIENZA EL PROCESO PARA SER DESIGNADA COMO ORGANISMO NOTIFICADO DE ACUERDO AL MDR