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S. 340

BillFederalSenateFloor Consideration
A bill to promote competition in the market for drugs and biological products by facilitating the timely entry of lower-cost generic and biosimilar versions of those drugs and biological products.
About This Bill
Introduced
Latest Action · February 6, 2019
Read the second time. Placed on Senate Legislative Calendar under General Orders. Calendar No. 22.
Congress
116th (2019–2021)
Introduced
February 5, 2019
Cosponsors (41)
22D 18R
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Summary

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Creating and Restoring Equal Access to Equivalent Samples Act of 2019 or the CREATES Act of 2019 This bill generally allows the developer of a drug or biological product, such as a generic or biosimilar version of a drug, to bring a civil action against the license holder of an approved medication if the holder refuses to make available sufficient quantities of the approved medication for the developer's testing. The bill also establishes affirmative defenses to such a civil action. In addition, the bill authorizes drug manufacturers seeking Food and Drug Administration approval for a generic drug to use alternative methods to develop elements assure safe use of a drug.

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