MHRA session on UK medical gadget regulation: Evaluation
Ian Bolland is joined by Ashleigh Batchen, Regulatory Affairs Supervisor from the British In Vitro Diagnostics Affiliation (BIVDA) to debate the MHRA’s printed session about how medical units and IVDs shall be regulated within the UK post-Brexit.
Additionally they contact upon experiences that may be learnt from the implementation of EU MDR and IVDR when transitioning to a brand new regulation and potential challenges alongside the way in which for producers, and in the case of notified physique capability.
You may learn the session right here: www.med-technews.com/information/Medtech-R…evice-regulat/
This podcast is sponsored by Area, a PTC Firm, for extra data go to: www.ptc.com/en/merchandise/area
