This facility will allow us to service every need of tier one medical device OEMs well into the future.
Mansfield, MA (PRWEB) July 18, 2007
Proven Process Medical Devices, a contract R&D and manufacturing firm specializing in electromechanical medical devices and equipment, including active implantable devices, has relocated their U.S. headquarters to a new 43,000-square-foot facility in Mansfield, Massachusetts. The location represents an 80% increase in total facility area over the company's former location in East Walpole, MA.
"The strategic move to dramatically increase our research, engineering and manufacturing space -- inclusive of a state-of-the-art Class 10,000 (ISO Class 7) clean room -- comes at a time of unprecedented demand for our categorical expertise, and growth in every area of our company," said Kenneth Fine, President of Proven Process Medical Devices. "This facility will allow us to service every need of tier one medical device OEMs well into the future."
Located in Mansfield's Cabot Business Park, Proven Process's expanded facility joins a "neighborhood" occupied by world-class biotech and medical device OEMs such as Tyco Healthcare Kendall and Smith & Nephew Endoscopy, which just last year dedicated an expanded campus in the business park.
Founded in 1994, Proven Process Medical Devices has provided innovative solutions for a wide variety of companies from high profile clients such as C.R. Bard, Boston Scientific, Johnson & Johnson, and Pfizer to emerging companies poised to make their names in the industry.
Proven Process is an FDA-registered and ISO 13485:2003 certified full-service outsourcing partner that provides exceptional design, development, validation and contract manufacturing services, exclusively for the medical device industry.
Visit Proven Process Medical Devices on the web at http://www.provenprocess.com.
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