ABHI Annual Regulatory Conference
From Directives to a Single Regulation
Register for the ABHI Regulatory Conference on 25 November in London. This is an opportunity to learn more about policy makers’ future plans so as to better prepare for new requirements.
Now that the summer break is over, the European Parliament is getting down to business and Medical Device legislation is high on the agenda. In parallel, the Member State Competent Authorities are actively debating what they would like to see in the new legislation. The EU Commission is reconstituting itself and we will soon know more about the shape of the new device Regulation.
For full programme details, click here.
Key Topics include:
• UDI
• Labelling
• Reprocessing and Sterilisation
• Clinical Evidence
• Responsibilities of economic partners
• Own Brand labelling
• Classification
Confirmed Speakers include:
John Wilkinson OBE
Director of Devices, MHRA
John Brennan
Director Regulatory and Technical Affairs, Eucomed
Dr Philippe Auclair
Senior Director, Regulatory Strategy & Advocacy, Abbott Quality & Regulatory EMEA, Abbott Laboratories
Peter Schroeer
Group Director EMEA Regulatory Affairs, Ethicon Endo-Surgery (Europe) GmbH
Dr Joachim Wilke
Director Regulatory, Medtronic
Click here to register now