7th Annual Medical Device Clinical Research Conference
Conference - Alexandria, VA, United States
Over the course of the past several years, regulatory authorities in both the US and abroad have begun to implement restrictions on the approval and clearance of medical technologies, resulting in a need for additional clinical evidence and long term efficacy information in order to support approval. At the same time, a period of economic uncertainty has also resulted in many healthcare professionals re-examining the products and technologies being used, in an effort to stem rising costs and the rate of medical interventions. These two pressures have changed the way in which manufacturers view, plan for, and execute clinical research on their devices and technologies, resulting in new challenges for clinical executives, as well as different priorities for clinical studies.
In addition to real-time case study presentations, tracked sessions and breakout round-table discussions will allow participants to discuss the key areas of concern within their teams; whether that is supporting evidence for a 510(k) or a PMA approval. Through covering a wide-variety of sessions for any type of device manufacturer, this conference will provide a one-stop opportunity for executives that need to reduce the time and cost of their medical device clinical trials.
Organization: Q1 Productions
(Courtesy of 7th Annual Medical Device Clinical Research Conference's logo, via q1productions.com)
7th Annual Medical Device Clinical Research Conference
21st - 22nd October 2013
Alexandria, VA, United States
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