Learning from big data: are we undertreating older women with high-risk breast cancer? [PDF]
, 2016 There is increasing interest in leveraging ‘big data’ to address important clinical questions, with the ultimate goal of improving human health, including outcomes for those with cancer.1 Examples include ‘CancerLinQ’, an initiative developed by the ...
Muss, Hyman, Sparano, Joseph A
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Federal Food, Drug, and Cosmetic Act - 20 Years of Health Protection [PDF]
, 1959 Twenty years of major public health protection have been provided since enactment of the Federal Food, Drug, and Cosmetic Act of 1938. The Food and Drug Administration, a constituent of the United States Department of Health, Education, and Welfare ...
Kerlan, Irvin
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Dietary Supplements: A Review of United States Regulation with Emphasis on the Dietary Supplement Health and Education Act of 1994 and Subsequent Activity [PDF]
, 2012 This paper undertakes a review of notable dietary supplement regulation in the United States. First, this paper discusses dietary supplements generally and their uses and economic characteristics.
Scarbrough, Brian
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Farm-Level Contracting for Production Process Attributes: An Analysis of rBST in Milk Production [PDF]
, 2021 On November 5, 1993, the Food and Drug Administration (FDA) approved Recombinant Bovine Somatotropin (rBST), also JOURNAL OF FOOD LAW & POLICY called Recombinant Bovine Growth Hormone (rbGH), for commercial use to increase milk production in dairy cattle.
Cook-Mowery, Clayton +2 more
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Sample Size Determination for Food Sampling
Journal of Food Protection, 2023 Industry and public health agencies sample and test food products for various purposes related to food safety and quality. Methods of sample selection and sample size determination are important in designing an optimal sampling plan.
Shizhen S. Wang +3 more
doaj
Specificity of HercepTest in Determining HER-2/neu Status of Breast Cancers Using the United States Food and Drug Administration–Approved Scoring System [PDF]
, 1999 Timothy W. Jacobs +4 more
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A survey of Top 200 Drugs—Inconsistent Practice of Drug Strength Expression for Drugs Containing Salt Forms [PDF]
, 2012 Many ionizable drugs are developed and marketed as salt forms. However, there are no clear US regulatory guidelines on drug strength labeling for salts. The strengths of some drugs are expressed as salts and some as free acids/bases.
Prohotsky, Daniel, Zhao, Fang
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United States Food and Drug Administration Approves Distribution of 10-Minute Flu Test to All Doctors [PDF]
, 2000 M. T. Osterholm
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August 23, 2013, 11:30 ET (11:30 AM ET)HANINFO-00354Summary: CDC now has an expanded access investigational new drug (IND) protocol in effect with the Food and Drug Administration (FDA) to make miltefosine available directly from CDC toclinicians for ...
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New Drug Research, The Extraterritorial Application of FDA Regulations, and the Need for International Cooperation [PDF]
, 2003 In recent years, U.S. pharmaceutical companies have expanded their new drug trials beyond the borders of the United States. While the companies have a variety of reasons for making this move, among them may be a desire to avoid Food and Drug ...
DuBois, William
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