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The Environmental Protection Agency (EPA) is an independent agency of the United States government tasked with environmental protection matters. [2] President Richard Nixon proposed the establishment of EPA on July 9, 1970; it began operation on December 2, 1970, after Nixon signed an executive order . [ 3 ]
The TSCA is found in United States law at Title 15 of the United States Code, Chapter 53, [14] and administered by EPA. Title of the TSCA, "Control of Toxic Substances," is the original substance of the 1976 act, establishes the core program, including regulation of polychlorinated biphenyl (PCB) products and bans certain activities with ...
The Medical Waste Tracking Act of 1988 was a United States federal law concerning the illegal dumping of body tissues, blood wastes and other contaminated biological materials. It established heavy penalties for knowingly endangering life through noncompliance.
Drug-testing a blood sample measures whether or not a drug or a metabolite is in the body at a particular time. These types of tests are considered to be the most accurate way of telling if a person is intoxicated. Blood drug tests are not used very often because they need specialized equipment and medically trained administrators.
The FDA requires nonclinical laboratory studies on new drugs, food additives, and chemicals to assess their safety and potential effectiveness in humans in compliance with 21 CFR Part 58, Good Laboratory Practice for Nonclinical Studies under the Federal Food Drug and Cosmetic Act and Public Health Service Act. [16]
Toxicology testing, also known as safety assessment, or toxicity testing, is the process of determining the degree to which a substance of interest negatively impacts the normal biological functions of an organism, given a certain exposure duration, route of exposure, and substance concentration.
In the United States, medical and food test products are regulated by the Food and Drug Administration (FDA). [1] [2]Title 21 "Food and Drugs" , Part 50 "Protection of Human Subjects" defines test article as "drug (including a biological product for human use), medical device for human use, human food additive, color additive, electronic product, or any other article subject to regulation ...
Drug checking or pill testing is a way to reduce the harm from drug consumption by allowing users to find out the content and purity of substances that they intend to consume. This enables users to make safer choices: to avoid more dangerous substances, to use smaller quantities, and to avoid dangerous combinations.