Webinar : MDR and MedTech Clinical Evaluation in Ireland

Two Day Webinar – 24th/25th Feb 2021

HRB-CRCI in conjunction with Enterprise Ireland will hold a webinar on Feb 24th & 25th addressing the Medical Device Regulations coming into force in May 2021.  The regulations will replace the existing Medical Device and Active Implantable Medical Device Directives.  Key changes include the importance of the Quality Management Systems (QMS) based upon the ISO standard ISO 13485 and the increased emphasis on clinical investigation.  These topics will be addressed along with input from our competent authority and a notified body.

There are four sessions over the two days. The full agenda and registration links for each session can be found in the document below –

MDR and MedTech Clinical Evaluation