Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Safety Federal Food, Drug

One major problem caused by Section 409 (c) (3) of the Federal Food, Drug and Cosmetic Act, commonly known as the Delaney Clause , which governed the registration of pesticides was the statement, No additive shall be deemed safe if it is found to induce cancer when ingested by man or animal,... . Dr Fred R. Shank, Director, Center for Food Safety and Applied Nutrition, US Food and Drug Administration, in... [Pg.60]

Personnel. More than any other area, we are often asked "How many people has your corporation added due to TSCA " I don t know of anyone who has a concise answer to this question. Complicating the situation is the fact that the 1960 s and 1970 s saw a number of environmental and health laws go into effect the Clean Air Act, Clean Water Act, Occupational Safety and Health Act, Safe Drinking Water Act, Federal Water Pollution Control Act, TSCA, Federal Food, Drug and Cosmetic Act, Hazardous Materials Transportation Act, Federal Insecticide, Fungicide and Rodenticide Act, Resource Conservation and Recovery Act, and Comprehensive Environmental Response, Compensation and Liability Act, to mention the major ones. This mixture of acts, with some similarities of purpose, developing within a time span of 10-15 years, has made a variety of similar demands. It is not easy at this point to attribute the addition of staff support personnel to an individual law such as TSCA. The same observation is applicable to all corporate resources which have felt the effects of TSCA however, in order to... [Pg.124]

The Food Drug Administration has the responsibility for the premarket clearance of all animal drugs. The 1958 food additive amendment to the Federal Food, Drug Cosmetic Act requires sponsors to demonstrate the safety of their products. The Kefauver-Harris amendment of 1962 requires the sponsors to demonstrate, in addition to safety, the efficacy of their drugs. Safety implies safety to the animal as well as to the consumers of animal products. The role of the Center for Veterinary Medicine in the premarket approval process is to establish conditions of drug use and to establish the allowable tolerances for drug residues in animal-derived food products. [Pg.128]

The Federal Food, Drug and Cosmetic Act (FFDCA) places the responsibility for establishing the safety and efficacy of human and veterinary drugs and devices and the safety of food and color additives on the sponsor of the regulated product. The Public Health Service Act requires that a sponsor... [Pg.11]

Under the terms of the US Food Regulations, flavourings fall under the definition of food additives. The respective definition was implemented in the Federal Food Drug and Cosmetic Act by the Food Additives Amendment of 1958. With this amendment, the general requirement of safety became the major topic for food additives. [Pg.20]

The Federal Food, Drug, and Cosmetic Act and the Code of Federal Regulations contain the basic framework for the regulation of food additives in the United States. Section 409 (c)(3)(A) of the Act requires that food additives must be safe for their intended uses before they can be intentionally added to food. 21 CFR 170.3 (i) defines safe or safety as ... [Pg.74]

If the Attorney General finds that the scheduling of a substance in schedule I on a temporary basis is necessary to avoid an imminent hazard to the public safety, he may, by order and without regard to the requirements of subsection (b) of this section relating to the Secretary of Health and Human Services, schedule such substance in schedule I if the substance is not listed in any other schedule in section 812 of this title or if no exemption or approval is in effect for the substance under section 505 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 355). Such an order may not be issued before the expiration of thirty days from —... [Pg.235]

The mission of the FDA is to enforce laws enacted by the U.S. Congress and regulations established by the Agency to protect the consumer s health, safety, and pocketbook.The Federal Food, Drug, and Cosmetic Act is the basic food and drug law of the United States. With numerous amendments, it is the... [Pg.265]

Health and Safety Factors. The LD5Q of anhydrous sodium thiosulfate for mice is 7.5 0.752 g/kg (40). Because of low toxicity, it can be safely used in veterinary medicine. Sodium thiosulfate pentahydrate is affirmed as a GRAS indirect and direct human food ingredient under the Federal Food, Drug, and Cosmetic Act (41) (see Food additives). [Pg.30]

Comprehensive Environmental Response, Compensation and Liability Act Dangerous Cargo Act Federal Coal Mining Safety Health Act Federal Food Drug Cosmetic Act Federal Insecticide, Fungicide Rodent Act Federal Water Pollution Control Act Hazardous Materials Transport Act Occupational Safety and Health Act Safe Drinking Water Act Toxic Substance Control Act... [Pg.228]

The ADI is usually set one hundred times lower than the no observable effect level (NOEL). A much greater safety factor is required if there is evidence that the pesticide causes cancer in test animals. Although the Delaney Amendment to the Federal Food, Drug, and Cosmetic Act prevents the addition of an animal carcinogen to foods, it does not apply to pesticide residues that occur inadvertently in the production of the crop. [Pg.44]


See other pages where Safety Federal Food, Drug is mentioned: [Pg.135]    [Pg.629]    [Pg.733]    [Pg.775]    [Pg.292]    [Pg.219]    [Pg.489]    [Pg.59]    [Pg.65]    [Pg.36]    [Pg.204]    [Pg.89]    [Pg.3]    [Pg.304]    [Pg.60]    [Pg.80]    [Pg.84]    [Pg.2]    [Pg.4]    [Pg.389]    [Pg.426]    [Pg.1262]    [Pg.413]    [Pg.532]    [Pg.6]    [Pg.22]    [Pg.94]    [Pg.832]    [Pg.349]    [Pg.1008]    [Pg.343]    [Pg.251]    [Pg.355]    [Pg.244]    [Pg.158]    [Pg.520]    [Pg.882]    [Pg.1867]   


SEARCH



Drugs safety

Federal Food, Drug

Food safety

© 2024 chempedia.info