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