The US Food and Drug Administration (FDA) has released a new draft guidance document aimed at providing clarity to the process by which certain designated medical gases become certified by regulators.

An Instagram ad catches your eye. You click to the product’s website and find reassurance: The product, it says, is "FDA certified" or was "produced in an FDA registered facility." Mention of the U.S.

This is an archived article and the information in the article may be outdated. Please look at the time stamp on the story to see when it was last updated. MINERVA, Ohio (WJW) – A local company has ...

The ANSI-ASQ National Accreditation Board (ANAB) recently notified the US Food and Drug Administration that LSQA SA of Montevideo, Uruguay now is accredited as a certification body (CB) by ANAB under ...

NEW YORK, Aug. 24, 2018 /PRNewswire/ -- The American National Standards Institute (ANSI), coordinator of the U.S. voluntary standardization system, has accredited the Perry Johnson Registrars Food ...

According to the Food and Drug Administration (FDA), the traditional paradigm of medical device regulation was not designed for adaptive artificial intelligence and machine learning technologies. As a ...

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We collaborate with the world's leading lawyers to deliver news tailored for you. Sign Up for any (or all) of our 25+ Newsletters. Some states have laws and ethical rules regarding solicitation and ...

FDA issued a proposed rule today to increase fees for color additive certification services. If finalized, it will implement a 10-cent-per-pound increase in color certification fees and revise the ...

Online HACCP Training Platform Delivers FDA/USDA/CFIA/GFSI-Compliant Certification That Qualifies Professionals for ...