Arena International's Clinical Operations and Outsourcing in Medical Device Trials Europe returns for its 2nd year. The 2015 conference will bring together leading clinical representatives from the medical device industries to discuss the biggest challenges within their clinical trials and outsourcing processes; a complex and ever-changing landscape.
Keynote Speakers:
- Gert Bos - Head of Regulatory and Clinical, BSI
- Charles-Thibault Burcez - Quality and Regulatory Affairs Manager, DEFYMED
- Alex Denoon - Partner, LAWFORD DAVIES DENOON
- Lynn Farrag - Clinical Operations and Clinical Project Manager, RANIER TECHNOLOGY LTD
- Karen Fraser - Senior Director, Clinical VENITI
- Dr. Toni Kennet Jorgensen - Head of Operation, Quality Assurance and Regulatory Affairs, SORIN GROUP
Key Presentations:
- Detailing requirements for a medical device trial juxtaposed with a pharmaceutical trial to streamline your trial effectively and curtail avoidable demands
- Avoiding disarray throughout your trial by establishing an effective management plan for multiple CROs
- Navigating through European regulatory bodies to ensure compliance and a reliable trial
- Investigating the changing regulatory landscape for medical devices disclosing expectations from regulatory bodies
- Developing effective procedures for study risk management in your medical device trial
Why attend Outsourcing Medical Device Trials?
The OCT series not only offers practical information to help drive down costs and improve trial quality but it allows attendees to get face to face with decision makers who can actually make a difference and influence trials moving forward. A must have date in the diary!
Quote reference code MK-MNT when booking your place
http://www.arena-international.com/omdteurope
Twitter: @ArenaIntOCT