One-shot devices, which are engineered for one-time use and are often subject to destructive testing, represent an important class of critical components in areas ranging from aerospace to biomedical ...

Engineers could avoid expensive redesigns by planning medical device testing early in development with expert guidance.

FDA uses a range of biocompatibility test data to evaluate medical devices before clearing or approving them for marketing. The growing use of FDA-recognized consensus standards facilitates this ...

STEMart announces the expansion of its genetic toxicology capabilities with the In Vivo Rat Micronucleus Test services.

Ottawa, Dec. 08, 2025 (GLOBE NEWSWIRE) -- The global medical device testing market size is calculated at USD 10.77 billion in 2025 and is expected to reach around USD 24.32 billion by 2034, growing at ...

NEW BRIGHTON, Minn.--(BUSINESS WIRE)--TÜV SÜD announces its plans to expand its Medical & Health Services (MHS) facilities in New Brighton, Minnesota, during a groundbreaking ceremony. This 20,000 ...

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Most medical device manufacturers know the importance of putting a product through rigorous cleaning and testing before it is released into the market. Standard sterility and biocompatibility tests ...

This article is a condensed version of an article that appeared in the November/December 2022 issue of Chip Scale Review. Adapted with permission. Read the original ...