Industry standards group AIM Global has released the latest version of its standard for the testing of non-implantable wireless medical devices, to help users and manufacturers better determine if ...
Some of the most challenging leakage-current-testing requirements are those for patient-monitoring devices—both invasive and noninvasive. Such testing can be time-consuming and expensive, so it is ...
Cyberattacks and data theft are a serious problem in many industries, but in healthcare the consequences could be physically dangerous or even deadly or enrich the pockets of bad actors on the dark ...
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, ...
UL Achieves ASCA Accreditation for Medical Device Testing from the U.S. Food and Drug Administration
NORTHBROOK, Ill., April 13, 2021 /PRNewswire/ -- UL, the global safety science leader, has received designation as an accredited ISO/IEC 17025 laboratory under the U.S. Food and Drug Administration ...
Eurofins Medical Device Services North America, part of a global network of over 20 medical device testing laboratories and a leading medical device solutions partner, recently launcheda GMPPFAS ...
Changes affecting the approval of medical devices in Canada are coming. Health Canada has released a notice on Proposed Changes to the Guidance on Recognized Standards for Medical Devices along with a ...
DUBLIN, April 13, 2021 /PRNewswire/ -- The "Medical Device Testing Market with COVID-19 Impact, By Services (Testing, Inspection, Certification), Sourcing, Technology ...
STEMart announces the expansion of its genetic toxicology capabilities with the In Vivo Rat Micronucleus Test services. NEW YORK, NY, UNITED STATES, January 26, 2026 ...
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