S. 5046, also known as the “FDA Modernization Act 3.0,” is a bill that requires the Secretary of Health and Human Services, through the Commissioner of Food and Drugs, to issue new regulations about nonclinical testing methods. This legislation mandates an interim final rule...
Simple Explanation
The FDA Modernization Act 3.0 is a new law that asks for rules to be made so that scientists can use new ways instead of animal testing to check if medicines are safe, but it might be confusing and cost money without telling everyone how much.