117th Congress
Sponsor: Rep. Anna Eshoo — D — CA
Reauthorizes Food and Drug Administration (FDA) user fee programs for certain drugs and devices, establishes requirements to increase diversity in clinical trials, and modifies requirements relating to the overall supply chain for drugs and devices. Specifically, the bill reauthorizes through FY2027 the FDA user fee programs for prescription drugs, medical devices, generic drugs, and biosimilars. The bill also requires the development of action plans...
Don't be sad- we've got your back. Just enter your email below and instructions on resetting your password will be sent to you.
×