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  • US HOLIDAY SCHEDULE

    All U.S. NAMSA offices and laboratories will be closed Monday, May 27, 2013 in observance of the national holiday.  If you have specific testing needs during this time please contact our Client Care group at 419-662-4850 (Northwood) or 419-662-4847 (Irvine).

     

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  • NAMSA Expands Laboratory in Irvine, California

    NORTHWOOD, OHIO, USA – March 26, 2013 – NAMSA, the world’s leading medical research organization, continues its steady growth with the expansion of its microbiology laboratory in Irvine, California. The newly expanded and state-of-the-art laboratory space will utilize the latest technology for microbiology and sterility assurance testing and will open in spring 2013.

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  • NAMSA Offering Remote Training Seminars

    NAMSA is delighted to announce the addition of remote training seminars.  NAMSA Remote Training Seminars provide high level content and industry expert analysis on prevailing global topics in the medical device industry.  The one hour phone conferences offer insight on regulatory and clinical issues and concerns medical device manufacturer’s encounter in their development process.
    We will be offering four seminars from April to July.  
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  • NAMSA to Sponsor and Speak at Biocompatibilty and Performance of Medical Device Symposium in Minneapolis

    NAMSA, the world's leading medical research organization, would like to invite you to join us at BPMDS 2013 for a rare gathering..

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  • NAMSA Sponsoring Conference on Best Practices for Biocompatibility and Performance of Medical Devices

    NORTHWOOD, OHIO – Jan. 8, 2013 – NAMSA, the world’s leading medical device research organization, is sponsoring a comprehensive symposium based on the definitive new book, “Biocompatibility and Performance of Medical Devices,” assembled by ANSM expert Dr. Jean-Pierre Boutrand, in London, England, February 12-14. This one-of-a-kind event offers attendees crucial insights on medical device testing.
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  • NAMSA expands state-of-the-art laboratory in Lyon, France

    NORTHWOOD, OHIO, USA – Oct. 15, 2012 – NAMSA, the world’s leading medical device research organization, continues its steady growth with an expansion of its state-of-the-art laboratories in Lyon, France.

    Increased demand for NAMSA’s biocompatibility and histopathology services has led the company to invest in building an additional 12,000 square feet for its facility, which increases its capacity in Lyon by roughly 30 percent.
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  • NAMSA acquires The Integra Group, expanding imaging and clinical services

    NAMSA, the world’s leading medical device research organization, has acquired The Integra Group, a preclinical and clinical research organization located near Minneapolis. The medical device research, regulatory approval and commercialization process is continuously taking longer and costing more.  Having breadth and depth in consulting, non-clinical and clinical services with experts in cardiovascular, orthopedic, ocular, neurologic, gastroenterologic, urologic, combination product and related medical devices can help manufacturers accelerate these development efforts.

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  • NAMSA Rebrands Business Unit in France

    NORTHWOOD, OHIO – June 1, 2012 – NAMSA, a world leading contract research organization for medical devices, announced that its French business unit, Biomatech, will now conduct business under the NAMSA brand name.
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  • NAMSA Expands ICP Offering

    February 21, 2012

    For several years, NAMSA has offered metal analysis by Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES). As NAMSA continues to make vast improvements in our facility and instrumentation, we are proud to announce that NAMSA will now also be offering Inductively Coupled Plasma Mass Spectrometry (ICP-MS).

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  • NAMSA Opens Frankfurt Office to Provide Clinical Trial and Regulatory Support

    February 8, 2012

    NAMSA, recently announced the opening of its newest office located near Frankfurt, Germany, which is staffed to provide clinical research and consulting services throughout Europe. This new location will serve clients seeking regulatory approval to market medical devices in Europe, in addition to providing regulatory and clinical trial support to European companies seeking clearance from the U.S. Food and Drug Administration.

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