Quest International: Quest Responds to the Surge in FDA Recalls by Strengthening Industry-Leading Field Corrective Action Services
Quest International's Expanded FCA Resources Offer Medical Device OEMs Timely, Reliable Support Amid Rising FDA RecallsIRVINE ...
Yahoo Finance23d
Arthrosurface Returns to it Roots Following Divestiture from Anika Therapeutics
arthrosurface company logo Arthrosurface ... Primo Medical Group is also ISO 13485:2016 certified and is a registered manufacturer with the Office of Defense Trade Controls Compliance.
Arthrosurface Returns to it Roots Following Divestiture from Anika Therapeutics
Executive management from Primo Medical Group along with others, combined to acquire Arthrosurface, Inc., a leading provider of joint restoration and preservation solutions for active patients, from ...
Medical Design and Outsourcing8d
Polymer Medical announces ISO 13485 certification
Polymer Medical has achieved ISO 13485:2016 certification, the standard for QMS in the medical device industry.
Business Insider4d
Spark Biomedical Sets Sights on Global Expansion with New ISO 13485 and MDSAP Certifications
Dallas, TX, Nov. 18, 2024 (GLOBE NEWSWIRE) -- Spark Biomedical, a leading developer of wearable neurostimulation devices, proudly announces the recent achievement of ISO 13485:2016 and MDSAP Quality ...
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UPM Biomedicals Launches FibGel™ the World’s First Injectable Nanocellulose Hydrogel for Medical Devices
Designed and manufactured under ISO 13485 standards in Finland and designed for medical applications, FibGel is poised to transform the fields of soft tissue repair, orthopedics, regenerative medicine ...
Stockhouse10d
Natera Announces Completion of Signatera(TM) Analysis from the CALGB (Alliance)/SWOG 80702 Randomized, Phase III Clinical Trial in Colorectal Cancer
Natera operates ISO 13485-certified and CAP-accredited laboratories certified under the Clinical Laboratory Improvement Amendments (CLIA) in Austin, Texas, and San Carlos, California. For more ...