The U.S. Food and Drug Administration (FDA) published an updated final guidance on the use of International Standard ISO 10993-1, “Biological evaluation of medical devices - Part 1: Evaluation and ...
Brinkman brings more than 15 years of experience in biological sciences and is known for her rigorous, clinically relevant approach to biological risk evaluation BOENNIGHEIM, Germany and LIGONIER, Ind ...
MILPITAS, Calif.--(BUSINESS WIRE)--SMI (Silicon Microstructures, Inc.) is pleased to announce that biocompatibility of IntraSense™ has been confirmed at a major medical device manufacturer.
Medical device manufacturers use cytotoxicity testing to help prove that devices that come into contact with the human body are biocompatible. Testing results are critical for gaining market access, ...
The main theme running through FDA's guidance on ISO 10993-1 is that every medical device should be assessed for its specific risk to the end user. Audrey Turley and Thor Rollins In June 1906, ...
TOLEDO, Ohio--(BUSINESS WIRE)--NAMSA ®, the world’s only Medical Research Organization (MRO) that accelerates medical device development through integrated laboratory testing, clinical research and ...
Researchers have developed a surface treatment that could improve the body’s acceptance of medical devices such as joint replacements and stents, according to a Chemistry World report. The method ...
The global medical device CRO market presents robust opportunities driven by rising demand for innovative devices amidst an aging populationDublin, Dec. 18, 2025 (GLOBE NEWSWIRE) -- The "Medical ...
Brinkman brings more than 15 years of experience in biological sciences and is known for her rigorous, clinically relevant approach to biological risk evaluation "We're thrilled to welcome Katie to ...
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