1 Nov 2017 : AMMI Global Expert Sharing Session on EUMDR

1 Nov 2017 : AMMI Global Expert Sharing Session on EUMDR

1 NOV 2017 : AMMI GLOBAL EXPERT SHARING SESSION ON EUMDR

Over 60 members and guests attended the AMMI Global Expert Sharing Session on EU Medical Device Regulations at E&O Hotel Penang on 1 November 2017. The objective of this event is to provide insight and facilitate discussion among AMMI Members and key stakeholders on the impact of the new Medical Device Regulations in Europe for the Medical Device Industry. The event started off with the Key Note Presentation on “Challenges and Expectations of the New Medical Device Regulations in Europe for the Medical Device Industry” by Mr Juergen Heil, Senior Vice President Quality & Environment Management, B. Braun Melsungen AG, Germany, This was followed by a Panel Discussion led by Mr Frank Ried, Director of Ried Q&C Consultancy. The distinguished panel members also included Mr Juergen Heil, Peter Porzler, Vice President, Medical & Health Service (MHS), Global Non-Active Medical Devices, TUV SUD and Mr Tony Low, Director of Quality Assurance & Regulatory Compliance, Commissioning Agents International .

Watch the video highlights here…