Essentials of European Medical Device Regulatory Affairs

Essentials of European Medical Device Regulatory Affairs 7 March 2019

Programme

Time

Presentation

Presenter

10:00 Registration and Coffee 10.30 Welcome 10.35 Introductions 10.45 Module 1: What is a Device?

Kevin Ashton

11:20

Module 2: Who is who

Neil Armstrong

11.45 12:00

Coffee break

Module 3: Legislation

Sarah Louise Gill

12:30

Module 4: Classification of devices

Neil Armstrong

13:00 Lunch 13:45

Module 5: Conformity Assessment

Neil Armstrong

14:45

Module 6: Device Labelling

Dhanashree Gokhale

15:15 Coffee break 15:30

Module 7: Clinical considerations

Neil Armstrong

16:00

Module 8: Post Marketing

Sinéad Farrell

17:00 Close of Meeting

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