Qmed, the Leading Global MedTech Industry Resource, Partners with Clarimed, to Provide the Medical Manufacturing and Healthcare Industry with FDA Reports on Adverse Events
Clarimed provides fact-based insights and reviews into product quality and performance to help patients, providers, manufacturers and others in the healthcare industry make informed decisions.
23 Apr, 2012, 09:00 ET
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.
"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.
The new resource, listed under DeviceMatters on the Qmed Resources page, provides Qmed users exclusive access to download reports by product code, device category, or by manufacturer. Users can find and download free reports on any device category or manufacturer. Full detailed reports are also available for a fee.
"Clarimed is the first company to classify adverse events and put them into context, and I am very pleased that UBM Canon and Qmed are helping to facilitate this service – it is revolutionary for the medtech industry," commented Steve Corrick, Senior Vice President of UBM Canon.
"Transparency of information with analytical insights not only heralds better quality, but also fosters innovation. DeviceMatters, in association with Qmed, enables medical device industry professionals to improve their R&D, manufacturing, quality and portfolio initiatives by providing insights into medical device quality, its impact, and how specific improvements can help save lives and improve market positioning," said Dr. Nora Iluri, Founder and CEO of Clarimed. "Our partnership with Qmed is very important. It allows us to leverage Qmed's strong platform and tremendous base to help DeviceMatters reports reach the right audience in the right context," said Dr. Iluri.
Dr. Iluri will be the Keynote Speaker during a luncheon presentation at the BIOMEDevice Boston conference and event on April 25. She will also be delivering a demonstration on DeviceMatters during the Innovation Briefs Theater on April 26. For the conference agenda and registration details, please click here.
Learn more and access the new resources on Qmed here.
Qmed is the world's ONLY 100% qualified medical device supplier directory, search engine and industry resource, created exclusively for OEMs actively researching and sourcing qualified suppliers, products, and services during the product design cycle. Powered by advanced keyword search and embedded with relevant supplier and industry content, rich media, and RFP opportunities, Qmed is the critical resource used to connect medical device OEMs with qualified suppliers. From medical contract manufacturers to stock component suppliers and medical device consultancies, Qmed's powerful search tool, directory, and white paper library serves only relevant, editorially screened supplier listings and resources to provide the most efficient supplier-sourcing experience for medical device OEMs. Qualified suppliers are determined by verification of the following criteria: currently working with medical device OEMs, exhibit at medical device industry trade shows, are GMP compliant, ISO 9000, and/or FDA–registered.
About UBM Canon
UBM Canon, the leading B2B media company dedicated exclusively to the global $3.0 trillion advanced manufacturing sector, helps support the flow of information, commerce and innovation in such sophisticated segments as medical devices and pharmaceutical development. UBM Canon also addresses cutting-edge developments in broader areas of advanced engineering design and manufacturing, and manufacturing processes and packaging. UBM Canon is part of UBM plc (UBM.L) a global provider of media and information services for professional B2B communities and markets.
DeviceMatters provides medical device insights and market research reports for industry professionals to foster innovation and quality improvements that matter. DeviceMatters insights help in understanding regulatory requirements and the current medical device landscape including approval specifics, post-market safety performance and typical device failure modes. DeviceMatters is currently the only site that provides adverse event reporting of medical devices based on unbiased and independent FDA data, among other sources. DeviceMatters is a Clarimed brand.
Clarimed is a first-of-its kind healthcare ratings agency and reference site empowering consumers and professionals with fact-based information to make informed decision about their healthcare. Clarimed's core analytics and ratings are based on official government data, among others, to provide the most helpful insights into healthcare product quality and performance. Founded by Dr. Nora Iluri, a Ph.D. from MIT and a former McKinsey consultant, Clarimed is headquartered in Silicon Valley. Clarimed is a division of Acelly LLC.
SOURCE UBM Canon
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