The 5th Annual Clinical Evaluations & Investigations for Medical Devices
Expert Advice on Clinical Issues Faced by the Medical Device Industry
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2010 Keynote Speaker Dr Herbert Lerner, FDA
'Update on Medical Device Clinical Legislation'
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Clinical follow-up for medical devices is getting stricter, costlier and taking longer. With the revision of the Directive 2007/47/EC, continual amendments to local requirements and ISO standards, you need to be quick to keep up with constant changes to regulations in this market.
This is the only medical device event that can provide you with all the regulatory and operational aspects of clinical evalautions and investigations for medical devices.
2010 Highlights
- We are delighted to welcome Herbert Lerner from the FDA who will deliver a read more
- Danielle Giroud, Chair of ISO 14155 working group, will report first hand on read more
- Notified Body Quick-fire Panel Session. read more
- Data Protection and Privacy Rules. read more
- Managing your Clinical Trials to Achieve Peak Performance and Efficiency. read more
- Clinical trials for drug device combination products. read more
- And that’s not all........ read more
Your expert speaker panel will include:
Your expert speaker panel will include:
Dr Herbert Lerner
Deputy Director- Clinical
FDA
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Anthony Wilkinson
Medical Director
Cook Medical
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Dr Hannah Patrick
Consultant Clinical Adviser
NICE
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Eric Vicaut
Director
URC Lariboisière/Saint-Louis
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Gert Bos
Head of Regulatory & Clinical Affairs
BSI Healthcare
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Sharon Barnett-Myers
Director Health Economics
Medtronic
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Danielle Giroud
Founder
WMDO
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Anna Heile
Senior Clinical Research Scientist
Codman & Shurtleff
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Sponsors
Exhibitors
Media Partners
Important Announcement
Sunday, 18th April 14.30pm
We would like to advise delegates and speakers that although at this time there is travel disruption this conference and the assoicated workshops will take place as scheduled.
Where and When?
21 Apr 2010 - 22 Apr 2010
Novotel Amsterdam
2010 Speakers
Chose from 3 New Conference Extras:
1. PRE CONFERENCE SYMPOSIUM – Tuesday 20 April
Project Management & Outsourcing during Clinical Trials
6 expert speakers will contribute to this full-day session dedicated to project management, outsourcing and contracting CROs.
2. EVENING SEMINAR – Wednesday 21 April
Using Clinical Evidence to Achieve Market Access & Reimbursement
Led by the European Reimbursement Director of Synergus, Elisa Maldonado-Holmertz
3. POST CONFERENCE WORKSHOP - Friday 23 April
Conducting Clinical Literature Reviews
Led by Jeanette Benaddi, CEO of Medvance.
2010 Sponsors
Poll
Which clinical-related topic is of most interest to you?
Please select an answer
Past Attendees
Reviews
"Well organised conference. The content was excellent, bringing up front the news for medical device regulations"
"Great refresher and opportunity to meet others sharing similar challenges"
"Very good opportunity to network"
