European Medical Device Clinical Trials Conference

Best Practices in Clinical Research, Resulting in Regulatory Compliance, Reimbursement and On-Time Completion.

October 20-21, 2008
Brussels, Belgium

In an increasingly competitive and global marketplace for medical devices, European companies are making tremendous strides in their clinical, regulatory and reimbursement policies resulting in stronger profits and tremendous growth. The Medical Device Trials Europe conference will focus on trends and challenges in conducting clinical trials, securing regulatory approval and managing reimbursement for companies competing across Europe and around the world. This program is most appropriate for VPs and Directors of Clinical Affairs from European medical device companies.

Conference Program Will Include:

Understanding Evolving Regulatory Standards and Impact of Changes to the Medical Device Directives
Rob Higgins
Regulatory Section Head
Medicines & Healthcare products Regulatory Agency (MHRA)

Improving Collection & Use of Health Economics Data Research in Medical Device Trials
Elisabeth George
Associate Director, Technology Appraisals
National Institute for Health and Clinical Excellence (NICE)

Site Selection & Management Strategies for Medical Device Clinical Trials
Carin Wensing
Senior Clinical Research Associate
Meditech Strategic Consultants B.V.

And many more...

For registration details please contact:
Paul Hernandez, Marketing Manager
PHernandez@Q1productions.com
312-602-9684