MEDICAL DEVICE
CLINICAL STUDIES ~ 2
Day Webcast

Webinar Date: To be announced
Webcast Ref: W5-8209
Fee: £300 + VAT

• The Regulatory Framework Applicable to Medical Device Studies
• Standards and Guidelines
• Clinical Evaluation ~ Literature Review
• Designing Pre Market and Post Market Studies
• Ethical Considerations Throughout Europe for Pre and Post Market Studies
• Regulatory Clinical Investigation Notifications
• Site Assessment and Initiation Visits
• How to Write a Final Study Report 
• Current Key Issues Affecting Medical Device Studies

ONCE YOU HAVE REGISTERED AND PAID ONLINE THE WEBCAST WILL BE AVAILABLE TO YOU FOR A 3 MONTH PERIOD.