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Homeownership Vesting Plan Act of 2009
Legislative Progress
Momentum (last 30 days)
0
score
0 actions · 0 new cosponsors · 0 votes
Speed vs cohort
0pct
0d open
vs 6,490 other HR bills in the 111th — cohort avg 44d
No CRS summary is available for this bill yet. The source title, actions, sponsors, and text versions below come from Congress.gov.
These links require the bill number to appear in the filing's source-reported specific issue text. Client expenses and lobbying-firm income are separate disclosure fields.
Filing registrants (1)
2009 · second_quarter · Science/Technology
Food and Drug Revitalization Act: to provide for reasonable limits for conflicts of interest on FDA advisory committees and to stimulate pediatric device development. Also, to include unique device identification systems for medical devices. H.R. 1356/S.540 - Medical Device Safety Act of 2009: to amend the Food, Drug and Cosmetic Act with respect to liability under state and local requirements for medical devices. H.R. 759 - The Food and Drug Administration Globalization Act of 2009: to provide for the safety of medical devices manufactured in foreign countries. H.R. 1548 - Pathway for Biosimilars Act: provides a pathway for the FDA approval of complex biological products from a reference product. H.R. 1427 - Promoting Innovation and Access Life-Saving Medicare Act: establishes a pathway for the FDA to approve more affordable copies of biotech and establish user fees for these products.
Bills with similar content found using semantic analysis.
Sources: Congress.gov
Client expense: $382,000 · Firm income: Not reported
Government targets: Centers For Medicare and Medicaid Services (CMS), Food & Drug Administration (FDA), HOUSE OF REPRESENTATIVES, Health & Human Services, Dept of (HHS), Medicare Payment Advisory Commission (MedPAC), SENATE
2009 · first_quarter · Science/Technology
Food and Drug Revitalization Act: to provide for reasonable limits for conflicts of interest on FDA advisory committees and to stimulate pediatric device development. Also, to include unique device identification systems for medical devices. H.R. 1356/S.540 - Medical Device Safety Act of 2009: to amend the Food, Drug and Cosmetic Act with respect to liability under state and local requirements for medical devices. H.R. 759 - The Food and Drug Administration Globalization Act of 2009: to provide for the safety of medical devices manufactured in foreign countries. H.R. 1548 - Pathway for Biosimilars Act: provides a pathway for the FDA approval of complex biological products from a reference product. H.R. 1427 - Promoting Innovation and Access Life-Saving Medicare Act: establishes a pathway for the FDA to approve more affordable copies of biotech and establish user fees for these products.
Client expense: $751,000 · Firm income: Not reported
Government targets: Centers For Medicare and Medicaid Services (CMS), Food & Drug Administration (FDA), HOUSE OF REPRESENTATIVES, Health & Human Services, Dept of (HHS), Medicare Payment Advisory Commission (MedPAC), SENATE