Related documents/summary of meetings
Contact

The Regulatory Issues Working Group will look at the regulatory environment for medical devices and public health in the UK, identify any issues which would benefit from joint working between Government and industry, both currently and in light of forthcoming regulatory developments, and agree a joint approach. In particular this will require consideration of:

• the developing relationship between the recently established Medicines and Healthcare products Regulatory Agency (MHRA) and the industry;
• the UK’s contribution to the EU and other international institutions on legislative proposals and discussions, particularly in connection with tissue engineering, the recent review of the Medical Devices Directives and promotion of standards;
• regulatory issues posed by emerging technologies and advances in information technology;
• transparency and provision of information about medical devices

This working group will be co-chaired by Dr David Jefferys, Head of the Devices Sector, MHRA and Mr Chris Hodges, Partner, Cameron McKenna

Summaries of meetings

• Note of First Meeting 18 December 2003
• Note of Second Meeting 29 January 2004
• Note of Third Meeting 1 March 2004

Recent papers originating from Working Groups

Contact

Steve Owen, MHRA: Steve.Owen@mhra.gsi.gov.uk

Paul Brice, MHRA: Paul.Brice@mhra.gsi.gov.uk

David Purnell, ABHI: david.purnell@abhi.org.uk

Clive Powell ABHI: clive.powell@abhi.org.uk

Membership

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