Healthcare is consistently one of the most attacked critical industries – it is a prime ransomware target. The reasons are ...
MRDC seeks entrepreneurs to help fast-track innovative new tools that reduce risks to patients and surgeons during complex ...
As we previously reported, agile licensing amendments to the Food and Drug Regulations and Medical Devices Regulations were registered on November ...
The Food and Drug Administration recently issued a Warning Letter concerning unauthorized modifications made to a previously cleared medical ...
Such medical device organisations can be involved in ... He has an excellent understanding of risk management, Post Market Surveillance (PMS) and vigilance. ResearchAndMarkets.com is the world's ...
Here's what to know about the recalls. A medical device is recalled when it fails to meet FDA standards or poses a health risk. Medical device companies typically will recall a product voluntarily ...
the U.S. FDA on Monday released separate draft guidance on the use of the technology in the development of new drugs and ...
University Risk Management refers all medical malpractice and patient related incidents, questions and concerns to the UAB Office of Risk Management and Insurance. Clinical risk management (medical ...
The Food and Drug Administration (FDA) published new guidance for AI-enabled medical devices on January 7, 2025. These are nonbinding and not for implementation. The public comment window for ...
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