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lobbying_activities: 908564

Individual lobbying activities reported in quarterly filings. Each row is one issue area for one client — includes the specific issues lobbied on, government entities contacted, and income/expense amounts.

Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API

This data as json

id filing_uuid filing_type registrant_name registrant_id client_name filing_year filing_period issue_code specific_issues government_entities income_amount expense_amount is_no_activity is_termination received_date
908564 08d890b8-9cce-44aa-a28a-cf112cee36c7 Q1 PARRY, ROMANI, DECONCINI & SYMMS 30792 AMERICAN ASSOCIATION FOR HEALTH FREEDOM 2010 first_quarter FOO FDA reform and legislation related to dietary supplements. H.R. 759, To amend the Federal Food, Drug, and Cosmetic Act to improve the safety of food, drugs, devices, and cosmetics in the global market, and for other purposes. H.R. 875, To establish the Food Safety Administration within the Department of Health and Human Services to protect the public health by preventing food-borne illness, ensuring the safety of food, improving research on contaminants leading to food-borne illness, and improving security of food from intentional contamination, and for other purposes. H.R. 2749, the Food Safety Enhancement Act of 2009, grants the Food and Drug Administration the authorities and resources it needs to better oversee the safety of the nation's food supply. S.510, the FDA Food Safety Modernization Act, granting the Food and Drug Administration additional authority and resources to better oversee the safety of the nations food supply. Legislation to allow growers of healthy foods and manufacturers of dietary supplements to cite legitimate scientific studies on the health benefits of these products without having them classified as unapproved new drugs. Actual legislation under development. Legislation in both the House and Senate to reform the health care system in the United States (H.R. 3962 and H.R. 3590). S. 3002, the Dietary Supplement Safety Act of 2010 that would repeal key sections of the DSHEA of 1994 and subject dietary supplements to increased regulation by the FDA. HOUSE OF REPRESENTATIVES,SENATE 30000   0 0 2010-04-07T12:07:10.680000-04:00
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