This webinar will provide participants with the latest developments regarding the preparation of harmonized standards (hENs) for Healthcare.
It will also provide guidance and solutions to Technical Bodies in the preparation of harmonized standards in support of the Medical Device Regulation (MDR) and the In Vitro Diagnostic Medical Devices Regulation (IVDR) to ensure a smooth citation of healthcare standards in the Official Journal of the European Union.
Target audience: CEN and CENELEC Technical Body Officers, experts involved in the development of harmonized standards in support of the Medical Device Regulation (EU) 2017/745 and In Vitro Diagnostic Medical Devices Regulation (EU) 2017/746 (IVDR).
Consult the draft agenda.