H. J. RES. 145 is a joint resolution aimed at expressing Congress's disapproval of a specific rule made by the Food and Drug Administration regarding "Medical Devices; Laboratory Developed Tests." This means that Congress does not agree with the rule, formally submitted on...
Congress doesn't like a new rule made by the FDA about how some medical tests are made and used, and they want to stop it from being put into action.
S. J. RES. 82 is a joint resolution allowing Congress to reject a rule issued by the Food and Drug Administration (FDA) concerning "Medical Devices; Laboratory Developed Tests." This resolution states that the FDA's rule, which was published in the Federal Register, would...
Congress is considering a special rule that would allow them to stop a new decision by the people who check if medical tests are safe. This means Congress might cancel a new rule about medical tests that aren't made in big factories, but they haven't explained why or what will happen next.
S. 3621 seeks to amend the Federal Food, Drug, and Cosmetic Act to establish nonvisual accessibility standards for devices with digital interfaces, particularly those used at home, ensuring they are accessible to people who are blind or have low vision. The bill defines a...
S. 3621 is a rule that tries to make gadgets with screens, especially those used at home, easier to use for people who can't see well or at all. It wants these gadgets to have special settings so that everyone can use them without changing how they work.
H.R. 9157, also known as the “Access to Pediatric Technologies Act of 2024,” aims to improve access to medical devices designed for children by providing a framework for establishing payment rates under Medicare. The bill instructs the Secretary of Health and Human Services...
H.R. 9157, called the "Access to Pediatric Technologies Act of 2024," is a plan to help kids get special medical tools by setting fair prices. It asks the government to make sure doctors can be paid properly when they use these tools for kids.
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