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MPs take evidence on regulation of medical implants

13 June 2012

Image of UK Parliament portcullis

The Science and Technology Committee holds the second evidence session of its inquiry into 'Regulation of medical implants'. 

Issues

At this meeting, the Committee will be seeking to understand the perspective of:

  • the implant manufacturers and the leading UK notified body which certifies medical implants (British Standards Institute)
  • the European Commission, who are currently working on a revision of the Medical Devices Directive
  • the Medicines and Healthcare products Regulatory Agency (MHRA) and the Department of Health.

Witnesses

Wednesday 13 June 2012, Committee Room 8, Palace of Westminster

At 9.15am

  • John Howlett, Head of Notified Body, British Standards Institute (Healthcare) (BSi)
  • Peter Ellingworth, Chief Executive, Association of British Healthcare Industries (ABHI)
  • Mike Kreuzer, Technical and Regulatory Executive Director, Association of British Healthcare Industries (ABHI)

At 10.15am

  • Jacqueline Minor, Director of Consumer Affairs, Directorate-General for Health & Consumers, European Commission

At 10.45am

  • Sir Kent Woods, Chief Executive, Medicines and Healthcare products Regulatory Agency (MHRA)
  • Lord Howe (Earl), Parliamentary Under Secretary of State, Department of Health

Further Information