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 ...
Eurofins Medical Device Services is setting new standards with the industry's first GMP PFAS testing and advanced PFAS Risk Assessments for medical devices. LANCASTER, Pa., December 02, ...
DUBLIN, April 13, 2021 /PRNewswire/ -- The "Medical Device Testing Market with COVID-19 Impact, By Services (Testing, Inspection, Certification), Sourcing, Technology ...
WAKEFIELD, Mass.--(BUSINESS WIRE)--TÜV SÜD, a trusted global partner offering a comprehensive portfolio of testing, certification, auditing, and advisory services, recently announced their acceptance ...
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 ...
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 contract research organization will launch an expanded ISO 18562 gas pathway testing program and ISO 10993-18 particulate ...
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 ...
As data-driven innovation profoundly changes every industry, the healthcare sector is also affected. Digital twins – virtual copies of physical devices – are essentially changing the ...
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 ...
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