Speeding Access to Already Approved Pharmaceuticals Act of 2017
Official title: To require the Food and Drug Administration to expedite review of pharmaceuticals that are approved for marketing in the European Union.
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Referred to the Subcommittee on Health.
Speeding Access to Already Approved Pharmaceuticals Act of 2017
This bill amends the Federal Food, Drug, and Cosmetic Act to require the Food and Drug Administration to facilitate the development and expedite the review of a new drug, biological product, or medical device that has been approved in the European Union.
- Introduced in House Formatted Text PDF Formatted XML
Cite this page
U.S. Congress. (2026). H.R. 2113: Speeding Access to Already Approved Pharmaceuticals Act of 2017. 115th Congress. Open America. https://openamerica.io/bill/115-HR-2113/
"H.R. 2113: Speeding Access to Already Approved Pharmaceuticals Act of 2017." 115th Congress, 2026, Open America, https://openamerica.io/bill/115-HR-2113/.
H.R. 2113, 115th Cong. (2026), https://openamerica.io/bill/115-HR-2113/.
[H.R. 2113: Speeding Access to Already Approved Pharmaceuticals Act of 2017](https://openamerica.io/bill/115-HR-2113/)