EU: CAMD (Competent Authorities for Medical Devices) publishes FAQs on the transition to the MDR and IVDR

CAMD, the umbrella organisation for authorities responsible for medical devices in Europe, has published documents on their website containing frequently asked questions about the transition period leading to the EU Regulation on Medical Devices (2017/745 MDR) and In-Vitro Diagnostics (2017/746 IVDR) coming into full effect. These documents address questions about how to handle medical devices and in-vitro diagnostics during the transition period.

MDR: http://www.camd-europe.eu/sites/default/files/media/documents/FAQ_MDR_180117_V1.0.pdf

IVDR: http://www.camd-europe.eu/sites/default/files/media/documents/FAQ_IVDR_180117_V1.0.pdf