AUSTIN, Texas--(BUSINESS WIRE)--atsec AB Stockholm, Sweden is thrilled to announce: We are the first IEEE Authorized Testing Facility! We've officially been approved as an IEEE Authorized Testing ...
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, ...
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 ...
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 ...
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 ...
The US Food and Drug Administration (FDA) has recognized three new standards related to software security on medical devices. The standards address taking a total product lifecycle (TPLC) approach to ...
India is introducing a standardized fee structure for medical device testing to replace inconsistent market rates and enhance ...
The Print on MSN
Why medical device makers are objecting to new govt draft rules on testing fees, sterilisation labelling
Draft amendment proposes fixed fee structure for testing medical devices at govt labs, and a requirement that manufacturers ...
Medtech firms are split over draft norms on standardised testing fees, with some backing transparency and others warning of ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results