ROYAL OAK, Mich., Sept. 26 /PRNewswire/ -- The Beaumont Technology Usability Center (BTUC) will offer training aimed at helping smaller and start-up medical technology companies speed their product commercialization process.
In December 2007, FDA regulators will join BTUC product-usability and human-factors experts to conduct a webinar focusing on effective methods for meeting FDA risk assessment requirements. In early 2008, the organizations will offer an expanded, one-day, hands-on seminar in Michigan to introduce methods for human factors and usability testing, for containing research and design costs, and for navigating regulatory approval processes.
"Many small medical device companies do not have the internal resources to focus on these topics and are often unaware of the risk management practices that regulators expect to see in a product approval application," says Steve Ebben, Vice President of Planning & Marketing for BTUC. "By teaming with the FDA, we can offer training that will help firms that are new to the medical device industry while providing a valuable resource for the Michigan economy."
BTUC plans to offer the seminar in other venues throughout 2008.
For more information about the training, contact Michael Tanner, Director of Commercialization Services, at 248-551-0567 or visit http://www.beaumontusability.com.
About The Beaumont Technology Usability Center (BTUC)
BTUC's mission is to advance excellence in healthcare by improving medical technology and its use. BTUC provides medical device and equipment manufacturers with product development services that improve patient safety, minimize the cost of product development, and shorten the time-to-market.
BTUC's multidisciplinary team of human factors engineers, clinical
technology engineers, and patient care specialists are affiliated with
Beaumont Hospitals, which comprises a 1,061-bed acad
|SOURCE The Beaumont Technology Usability Center|
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