RUTTER Andrew J.

Andrew is a Manager, Regulatory Affairs Specialist within the Regulatory Affairs Team at Ortho-Clinical Diagnostics, and is based in their UK Operations Facility in Pencoed, South Wales. Andrew has more than 18 years experience in the IVD industry, having previously worked for Gen-Probe Inc. (now Holigic) where he held the position of Quality Assurance and Regulatory Affairs Manager, and also fulfilled the role of European Authorised Representative. Andrew has worked very closely with MedTech Europe for several years particularly with Unique Device Identification, serving as the Chairman of the UDI Group, and is the IVD representative on the European Commission’s EUDAMED Steering Committee.
Andrew has a BSc (Hons) and PhD in Biochemistry from Cardiff University.