Medical Product Communications Act of 2017
Official title: To amend the Federal Food, Drug, and Cosmetic Act with respect to determining the intended use of drugs and devices.
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Referred to the Subcommittee on Health.
Medical Product Communications Act of 2017
This bill amends the Federal Food, Drug, and Cosmetic Act to state that the intended use of a drug, biological product, or device shall be determined by the objective intent of the manufacturer and sponsor of such drug, biological product, or device, as demonstrated by statements contained in labeling, advertising, or analogous oral statements.
The intended use of these medical products shall not be determined by actual or constructive knowledge of the manufacturer or sponsor that these products will be used in a manner that varies from the use approved for marketing.
Additionally, the scientific exchange of information about these products shall not constitute labeling, advertising, or evidence of a new intended use. The bill sets forth the requirements for a scientific exchange.
- Introduced in House Formatted Text PDF Formatted XML
Cite this page
U.S. Congress. (2026). H.R. 1703: Medical Product Communications Act of 2017. 115th Congress. Open America. https://openamerica.io/bill/115-HR-1703/
"H.R. 1703: Medical Product Communications Act of 2017." 115th Congress, 2026, Open America, https://openamerica.io/bill/115-HR-1703/.
H.R. 1703, 115th Cong. (2026), https://openamerica.io/bill/115-HR-1703/.
[H.R. 1703: Medical Product Communications Act of 2017](https://openamerica.io/bill/115-HR-1703/)