Technical & Regulatory Forum
This is the main group for feedback to members on all issues of
concern in the Technical & Regulatory area.
Membership is open to all members.
Meetings usually take the form of presentations from guest
speakers on current topics of interest as well as updates on more
general issues from the ABHI staff.
Presentations at the Technical & Environment Forum held on
30th November 2007 were:
- Revision of MEDDEV 2.12-1 - Guidance on
Vigilance, Tony Sant, MHRA
- AIDC, Mike Kreuzer, ABHI
- Environment Update, Clive Powell, ABHI
- Revision of the Medical Devices Directive -
Update & Implications, Richard Gutowski, MHRA
- Global Labelling Requirements for Medical
Devices, Part 1 - Jim Willmott, Smiths Medical
- Global Labelling Requirements for Medical
Devices, Part 2 - Jim Willmott, Smiths Medical
For more information or if you would like to participate in this group, please contact us.