legislation: 117-s-4391
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
This data as json
| bill_id | congress | bill_type | bill_number | title | policy_area | introduced_date | latest_action_date | latest_action_text | origin_chamber | sponsor_name | sponsor_state | sponsor_party | sponsor_bioguide_id | cosponsor_count | summary_text | update_date | url |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 117-s-4391 | 117 | s | 4391 | CLEAR Documentation Act | Foreign Trade and International Finance | 2022-06-14 | 2022-06-14 | Read twice and referred to the Committee on Health, Education, Labor, and Pensions. | Senate | Sen. Cassidy, Bill [R-LA] | LA | R | C001075 | 0 | Correcting a Lack of Efficient, Adequate, and Reasonable Documentation Act or the CLEAR Documentation Act This bill establishes certain rules for the Food and Drug Administration to issue export certifications for medical devices that are manufactured outside of the United States. A certification for a medical device must be subject to a user fee. | 2022-12-29T17:48:36Z |