Programme

Clinical Evaluation of Medical Devices 6 th – 8 th November 2017

TOPRA Office, 6 th Floor, 3 Harbour Exchange, South Quay, London E14 9GE

Module Leaders: Vincent Legay

Monday 6 th November 2017

Chairperson

13.00

Registration

13.15 – 13.30 13.30 – 15.30

Welcome & Introduction To the Module Lecture 1: From EU MDD 93.42 to EU Medical Device Regulation 2017/745: Impact overview for Clinical Evaluation

Vincent Legay Vincent Legay NAMSA

15.30 – 16.00 16.00 – 17.45

Break

Beata Wilkinson CROMSOURCE

Lecture 2: Increasing obligations for manufacturers: impact on industry (tracing the changes 2.7/1 rev.3 to rev. 4 to MDR)

17.45 – 19.00

Introduction to Case Study

19.00

Wine reception

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