Conference Date: 09-13 Jul 2012
Conference Ref: N7-8012
Fee: £3350 + VAT
Venue: The Rembrandt Hotel, London
REASONS TO ATTEND
Learn what regulations control the manufacture and marketing of a device in the EU
Discover how regulatory, quality, clinical and other aspects of device development are joined into a continuous process.
Understand how a device obtains the CE Mark.
Social programme includes a conference dinner and theatre trip
Bringing a Medical Device to the market place is a complex and lengthy procedure which requires experience, knowledge and specialist skills. The contribution to successful market placement comes from many different skilled individuals and organisations. Those contributing towards the placing of devices on the market should be aware of all of the stages involved and be able to relate their responsibilities to the needs of other professionals, scientists, clinicians and regulatory and quality experts.
There will be ample time for informal discussions alongside the presentations and workshops.
This is a five day residential course and the registration fee will include 4 nights accommodation, all meals including the conference dinner and a trip to the theatre. A non-residential rate is available.