J. Keller’s new CTRE™ program offers fleet professionals advanced, hands-on training in the Federal Motor Carrier Safety Regulations, including driver qualification, hours-of-service, vehicle ...
Process AI in Medical Devices: What Works and What's Next, Upcoming Webinar Hosted by Xtalks ...
ANSI/AAMI HE75:2025; Human factors engineering - Design of medical devices is the first update to AAMI's premier human factors standard since 2009. The standard is meant to assist users and ...
Despite the rapid invention and widespread use of artificial intelligence (AI), the federal government is just beginning to shape the ...
The medical device industry faces growing pressure to align U.S. and EU regulations, with the EU’s Medical Device Regulation ...
Abstract: Learning and optimizing complex skills in disciplines such as golf is mainly based on the work of human trainers. Technology-based options such as video analysis and motion capturing are ...
Duty Of Disclosure Considerations For Medical Device Patent Applicants With Parallel FDA Submissions
Understanding the crucial overlaps between FDA disclosures and patent law is important for medical device innovators seeking ...
(MENAFN- GlobeNewsWire - Nasdaq) The evolving EU MDR and IVDR present key opportunities for companies to enhance compliance strategies, engage with notified bodies, and optimize market access. Staying ...
Patients with implanted medical devices like orthopedic joint replacements, pacemakers, and artificial heart valves run a ...
An accelerated regulatory pathway in Mexico has positioned the country as a priority launch market for medical devices. Guerreschi: This pathway is designed to reduce approval timelines by the Federal ...
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