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Qmed, the Leading Global MedTech Industry Resource, Partners with Clarimed, to Provide the Medical Manufacturing and Healthcare Industry with FDA Reports on Adverse Events
Date:4/23/2012

LOS ANGELES, April 23, 2012 /PRNewswire/ -- Qmed.com, the world's only 100% qualified medical device supplier directory, search engine, and central industry resource, today announced a partnership with the industry's only site that provides ground-breaking detailed reports of industry-related adverse events, DeviceMatters.  

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"We are thrilled to provide Qmed users and the medtech industry with FDA reports that provide key insights into adverse events and medical device failures in the industry.  The reports found on Clarimed's website DeviceMatters can also act as an early warning system for OEMs and product development in the future," stated Tim Simone, Qmed Brand Director.

Clarimed has recently uncovered that over 330,000 medical device adverse events with patient outcomes were reported to the FDA in 2011 alone. This is a sharp increase from only 3 years ago. Adverse event reports are filed when somebody has been injured or could have been injured while using a medical device. These reports do not prove that a device caused the injury, but it does provide a sense for how much risk is involved in using medical devices.  Clarimed's overall goal is to help industry professionals understand regulatory requirements and the current medical device landscape including approval specifics, post-market safety performance and typical device failure modes.

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