So, what's the deal with this new FDA Act 3.0? I'm all for modernization, but I'm not sure about the long term effects. What do you think?
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The bill H.R. 2821 in the 119th Congress, introduced on April 10, 2025, aims to mandate the Secretary of Health and Human Services, working with the Commissioner of Food and Drugs, to issue a conclusive regulation concerning nonclinical testing methods.
How will this impact me? ✨
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