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Animal drugs

S. F. Sundlof, J. E. Riviere, and A. L. Craigmill, Food Animal Residue Avoidance Databank (FARAD) Trade Name File, A Comprehensive Compendium ofi Food Animal Drugs, University of Florida, Gainsvihe, 1988. [Pg.161]

When it approved the New Animal Drug AppHcation (NADA) of formalin, FDA ruled that use of formalin for fisheries was safe for humans and the environment. They ruled that effluents from fish treatments at 250 mg/L should be diluted 10 times and from egg treatments 75 times if 1,000 —2,000 mg/L were used (10,11). Before registering the compound, FDA also addressed carcinogenicity by stating it was not concerned about human exposure from either water or fish treated with formalin. The U.S. Fish and Wildlife Service (USFWS) has procedural guidelines that should protect workers from harm fill levels of formalin. Calculations based on treatment levels demonstrated that a fishery worker is exposed to not more than 0.117 mg/L formalin in the air, well below the levels estabUshed by the U.S. Occupational Safety and Health Administration to protect workers. [Pg.322]

Subchapter F—New Animal Drugs for Minor Use and Minor Species... [Pg.13]

SEC. 571. CONDITIONAL APPROVAL OF NEW ANIMAL DRUGS FOR MINOR USE AND MINOR SPECIES. [Pg.13]

SEC. 572. INDEX OF LEGALLY MARKETED UNAPPROVED NEW ANIMAL DRUGS FOR MINOR SPECIES. [Pg.13]

Parts 500 to 599. Animal drugs, feeds, and related products. [Pg.14]

Caution. Contains a new animal drug for use only in investigational animals in clinical trials. Not for use in humans. Edible products of investigational animals are not to be used for food unless authorization has been granted by the U.S. Pood and Drug Administration or by the U.S. Department of Agriculture. [Pg.135]

Figure 7.1 Information supplied to the CVM in support of a Notice of Claimed Investigational Exemption (NCIE) for an Investigational New Animal Drug (INAD). Figure 7.1 Information supplied to the CVM in support of a Notice of Claimed Investigational Exemption (NCIE) for an Investigational New Animal Drug (INAD).
Depending on whether it is classified as a drug or a biologic, the applicant must submit either a New Animal Drug Application (NADA) to the FDA CVM or veterinary biologies licence applications to the USDA CVB. [Pg.144]

INSTRUCTIONS FOR PREPARING ANO SUSMITTING THE NEW ANIMAL DRUG APPLICATION... [Pg.145]

Number the pages ol Ihe new animal drug application. Each copy should bear the same page numbering. [Pg.145]

The EU regulations permit veterinarians to treat animals with animal drugs that have not been authorised for that species or, alternatively to use human drugs, in situations where there is no authorised drug for treatment of the condition in the species. [Pg.154]

Ator NA, Griffiths RR Principles of drug abuse liability assessment in laboratory animals. Drug Alcohol Depend 70(suppl) 55—72, 2003... [Pg.176]

Griffiths, RR. Brady, J.V. and Bradford, L.D. Predicting the abuse liability of drugs with animal drug self-administration procedures Psyehomotor stimulants and hallueinogens. Adv Behav Pharmacol 2 163-208, 1979. [Pg.40]

The process of development and validation of animal drug residue methods for US Food and Drug Administration regulatory use... [Pg.77]

C. Principles. The physical and chemical principles of the method should be described. The structure of the new animal drug should be provided. [Pg.87]


See other pages where Animal drugs is mentioned: [Pg.84]    [Pg.86]    [Pg.13]    [Pg.14]    [Pg.14]    [Pg.130]    [Pg.135]    [Pg.135]    [Pg.144]    [Pg.145]    [Pg.146]    [Pg.146]    [Pg.147]    [Pg.153]    [Pg.153]    [Pg.159]    [Pg.357]    [Pg.77]    [Pg.78]    [Pg.78]    [Pg.78]    [Pg.79]    [Pg.80]    [Pg.80]   


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Abbreviated New Animal Drug Application ANADA)

Abbreviated new animal drug application

Administration, animal health drugs

Animal Drug Amendments

Animal Medicinal Drug Use Clarification Act

Animal Models of Xenobiotic Nuclear Receptors and Their Utility in Drug Development

Animal drug 30 Contamination

Animal drug residue immunoassay

Animal drug residue immunoassay development

Animal drug residue methods

Animal drug-metabolizing enzyme activities

Animal health drugs

Animal models drug withdrawal

Animal sources, drugs from

Animal studies anticholinergic drugs

Animal studies drug development

Animal studies quantitative drug metabolism

Animal studies training drug doses

Animal studies, preclinical drug testing

Animals drug research

Animals in drug development

Communication animal health drugs

Drug abuse animal models

Drug approval process animal testing

Drug approval process animal trials

Drug biotransformation animal species

Drug development animal testing

Drug product animal-derived materials

Drug-induced liver injury animal models

Drugs and animal

Drugs animal testing

Drugs residues in animal products

Drugs testing, using animals tissues

Effects of drugs in animals

FDA Enforcement Methods for Drug Residues in Animal Food Products

Investigational new animal drug

Livestock, animal health drugs

New animal drug application

New animal drug application NADA)

Ocular drug delivery animal studies

Office of New Animal Drug Evaluation

Pharmaceuticals animal drugs

Preclinical drug development animal models

Safety animal drug residue methods

Test substances animal health drugs

Therapeutic drugs animal models

Transgenic animals humanized drug receptors

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