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TOLEDO, Ohio, March 3, 2025 /PRNewswire/ -- NAMSA, a leading US based MedTech testing, clinical and regulatory consulting firm, announced that it finalized its acquisition of WuXi AppTec's US ...
Medical device testing is vital as manufacturers need to comply with stringent regulatory standards ... The list includes companies offering a range of services, including but not limited to: Medical ...
Studies show that between 2008 and 2017, more than 83,000 deaths and 1.7 million injuries were related to faulty medical devices in the U.S. alone. 1,2 These failures could have been prevented with ...
“The monitoring of the quality of imported drugs, cosmetics, and medical devices is of paramount importance to public health,” states the document. It outlines a three-tier system for inspections, ...
This document has been published in the Federal Register. Use the PDF linked in the document sidebar for the official electronic format.
Limited validation expertise: The complexity of medical device testing necessitates specialised expertise for validation projects. However, only a few CROs and medical device manufacturers possess the ...
However, the microbiology testing will be mainly for syrup ... The international health agency also indicated that up to two billion people around the world lack access to necessary medicines, ...
As director of microbiology at Eurofins Medical Device Testing, Liz Sydnor oversees the microbiological testing of medical ... how do you think medtech engineers/scientists can stay ahead of the curve ...
The need for appropriate infrastructure to test medical devices is ... laboratories operating under concerned medical devices sector to ensure that necessary infrastructure & qualified human ...
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