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8th Annual European Medical Device Clinical Research Conference



 
Our Price: $495.00

Product Code: 2251
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About the Product
Includes presentation materials from the conference. Presentations slides are in PDF. format. All files are available for immediate download.

About the 8th Annual European Medical Device Clinical Research Conference

Achieving Clinical Research Budget Planning & Management, Implementing Flexible Trial Design in Light of the Upcoming MDR & Transition Period all while Streamlining & Expediting Regulatory Submission Operations

As medical technology has continued to rapidly evolve in design and complexity, the effective conduct of clinical research to support regulatory clearance of products has progressed in tandem, with new regulatory requirements focused on greater levels of data demonstrating the clinical efficacy and safety of the product. In a resource constrained environment focused on maximizing the outcome of each study, forward thinking clinical research executives are implementing creative strategies within study design and execution that ultimately streamline timelines and maintain expenditure. Through an examination of the ongoing progression of medical device clinical research in Europe, with special emphasis on forward-thinking, budget conscious decision making, the 8th Annual Q1 European Medical Device Clinical Research conference continues to provide executives with an unparalleled educational opportunity.

Unique to the 2015 conference agenda were a number of hands-on workshop formatted sessions, which provided participants with an opportunity for practical learning, knowledge share, and engagement with presenters and fellow attendees. With topics covering all of the major challenges of clinical executives; from utilization of adaptive trial design to meet internal and external stakeholder expectations to the ongoing impact of MDR implementation and varied interpretations of the regulation, the program continues to meet the high-level demands of clinical executives. As always, the program melded varied perspectives, including leading industry practitioners, notified bodies, competent authorities and study investigators, that ensured all perspectives were integrated into the meeting content.


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