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FTC Issues Updated Health Products Claims Guidance | MoFo Life Sciences

On December 20, 2022, the Federal Trade Commission (FTC) issued its Health Products Compliance Guidance (“Health Products Guidance”). This is the first update in nearly 25 years to. ....

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EU MDR And IVDR Implementation: European Commission Publishes Full Proposal For Amending Transitional Regime | MoFo Life Sciences

Following up on its announcement in the EU Employment, Social Policy, Health and Consumer Affairs Council (EPSCO) Meeting, the European Commission (Commission) released on January 6,. ....

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Congress Expands FDA Authority Over Cosmetics Regulation | MoFo Life Sciences

The Modernization of Cosmetics Regulation Act of 2022 (MoCRA) was passed by the U.S. Congress as part of the omnibus Consolidated Appropriations Act enacted on December 29, 2022 and. ....

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FDA Clarifies The Human Factors Or Usability Information To Include In A Device Marketing Submission | MoFo Life Sciences

If you are a device manufacturer, what human factors and usability information should you include in your marketing submission? What if your device has the same user interface as an. ....

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EU MDR And IVDR Implementation: Signs Of Relaxing Transitioning Regime And Bridging Measures | MoFo Life Sciences

Concerns over possible medical device shortages in the EU have led to two recent developments that will affect the implementation of the Medical Device Regulation (MDR) and In Vitro. ....

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