home / openregs / legislation

legislation: 109-s-3175

Congressional bills and resolutions from Congress.gov, filtered to policy areas relevant to environmental, health, agriculture, and wildlife regulation.

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
109-s-3175 109 s 3175 Life-Saving Medicines Export Act of 2006 Commerce 2006-05-25 2006-05-25 Read twice and referred to the Committee on the Judiciary. (text of measure as introduced: CR S5247-5252) Senate Sen. Leahy, Patrick J. [D-VT] VT D L000174 0 Life-Saving Medicines Export Act of 2006 - Allows the Director of the U.S. Patent and Trademark Office (USPTO) to issue a compulsory license to a generic manufacturer of a pharmaceutical product or a patented product needed to prevent or treat potentially life threatening public health problems for the purposes of manufacturing and exporting such pharmaceutical products to an eligible country. Allows exportation to a country that is a least developed country as designated by the United Nations (U.N.) or a country that lacks sufficient manufacturing capacities to produce the pharmaceutical product. Sets forth application requirements for compulsory licenses, including that the manufacturer sought a voluntary license from the patent holder. Requires the Director to establish an office within USPTO to assist applicants and eligible counties, nongovernmental organizations, or nations likely to become eligible countries in identifying companies in the United States which could provide pharmaceutical products under this Act. Sets forth formulas for calculating the royalty amount that the holder of a compulsory license must pay to the patent holder. Allows the Director to grant a compulsory license to a generic manufacturer on an expedited basis for a limited period for a pharmaceutical product to address a national emergency or other circumstances of extreme urgency. Declares that it is not patent infringement to manufacture and export a pharmaceutical product in accordance with this Act. Requires the Director to establish the National Advisory Board on Implementation of the General Council Decision to provide advice and guidance regarding the implementation and administration of the compulsory licensing program established under this Act. 2023-01-13T04:50:57Z  

Links from other tables

  • 3 rows from bill_id in legislation_actions
  • 25 rows from bill_id in legislation_subjects
  • 0 rows from bill_id in legislation_cosponsors
  • 0 rows from bill_id in cbo_cost_estimates
Powered by Datasette · Queries took 3.709ms · Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API