Proving your product to be safe and effective while also getting buy-in from the healthcare ecosystem are only some of the ...
The National Association of Boards of Pharmacy (NABP) plays an important role in the state licensing of prescription medical device manufacturers ...
GlobalData on MSN1d
Nearly a third of FDA medical device adverse event reports filed lateA new study found that 9.1% of medical device AEs were reported to the FDA 180 days later than required over a three-year ...
More than 1.2 million medical device adverse event reports were not submitted to the US Food and Drug Administration (FDA) ...
As of late February, there were 147 medical device recall events and 20 of them, or 13.6%, were Class I, according to a Modern Healthcare report.
MethodSense says it is helping pulse oximeter manufacturers with FDA draft guidance to enhance accuracy across diverse skin ...
These convictions should make one thing clear: corporate fraud that puts public health at risk will not go unpunished,” ...
Archimedic, a medical device development firm that provides Design, Regulatory, and Go-to-Market services to its clients, has ...
Medical consumables company Poly Medicure Ltd on Tuesday (March 11) announced that it has received Medical Device Regulation ...
Over 1.2 million medical device adverse event reports were not submitted to the US Food and Drug Administration (FDA) within the deadline set by federal regulations, finds an analysis of recent data ...
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