Veterinary Drug definition

Veterinary Drug means anysubstance applied or administered to any food-producing animal, such as meat or milk-producing animals, poultry, fish or bees, whether used for therapeutic, prophylactic or diagnostic purposes or for modification of physiological functions or behavior.
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Veterinary Drug means a drug sold for veterinary use, and includes a drug supplied on a prescription given by a veterinary surgeon;
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Veterinary Drug means any of the following:
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Examples of Veterinary Drug in a sentence

  • For more information, please also refer to the FDA guidance entitled Guideline for the Submission of Documentation for Sterilization Process Validation in Applications for Human and Veterinary Drug Products.

  • Toxicity of 17β-estradiol (E2)Various expert bodies have recognized that E2 is a potential carcinogen (WHO 2000 (Toxicological Evaluation of Certain Veterinary Drug Residues in Food.

  • Ovadine™ is currently (2007) under review by the Veterinary Drug Directorate for approval as a fish egg disinfectant.

  • Information related to the validation of the sterilization process need not be submitted at this time but should be submitted at the time of an NDA filing (see FDA guidance Submission Documentation for Sterilization Process Validation in Applications for Human and Veterinary Drug Products).

  • Information related to the validation of the sterilization process need not be submitted at this time but should be submitted at the time of an NDA filing (see FDA guidance for industry Submission Documentation for Sterilization Process Validation in Applications for Human and Veterinary Drug Products).

  • In particular, review of decisions may be necessary if they pose difficulties in the application of the Guidelines for the Establishment of a Regulatory Program for the Control of Veterinary Drug Residues in Foods.

  • For example, VICH GL-10(R) Impurities in New Veterinary Drug Substances recommends thresholds for the identification and qualification of organic impurities for synthetic new drug substances.

  • Information should be submitted as described in FDA’s “Guidance for Industry: For the Submission Documentation for Sterilization Process Validation in Applications for Human and Veterinary Drug Products” dated November 1994 (Ref.

  • Procedures Labor, Commerce and Industry 4926 Compounding of Veterinary Drug Preparations Regulations and Admin.

  • It noted that the Guidelines would supersede the Guidelines for the Establishment of a Regulatory Programme for Control of Veterinary Drug Residues in Foods (CAC/GL 16-1993) and Code of Practice for Control of the Use of Veterinary Drugs (CAC/RCP 38-1993).


More Definitions of Veterinary Drug

Veterinary Drug means any substance applied or administered to any food- producing animal whether used for therapeutic, prophylactic or diagnostic purposes or for modification of physiological functions or behaviour;
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Veterinary Drug means any substance applied or administered to any food- producing animal, poultry, fish, and bee, whether used for therapeutic, prophylactic, or diagnostic purposes, or for modification of physiological functions or behavior.
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Veterinary Drug means any substance, hormone or biological material which is used in the diagnosis, treatment or control of any veterinary disease, and this term includes any protein, salt or vitamin to be used in feed.
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Veterinary Drug means a drug used or intended or represented to be used as a drug for the treatment, prevention or diagnosis of a disease of an animal, and includes a drug listed or included by reference in the regulations;
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Related to Veterinary Drug

  • veterinary surgeon means a veterinary surgeon within the meaning of the Veterinary Surgeons Act 1936.

  • Medical marijuana product means a product that contains cannabinoids that have been extracted from plant material or the resin therefrom by physical or chemical means and is intended for administration to a licensed patient, including but not limited to concentrates, oils, tinctures, edibles, pills, topical forms, gels, creams, and other derivative forms, except that this term does not include live plant forms.

  • Generic Drug means any Prescription Drug approved by the FDA that has the same bio-equivalency as a specific Brand Name Drug.

  • Clinical laboratory means a facility for the microbiological, serological, chemical, hematological, radiobioassay, cytological, immunohematological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of a disease or assessment of a medical condition.

  • Participating Clinical Laboratory means a Clinical Laboratory which has a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan to provide services to you at the time services are rendered.

  • Tobacco product manufacturer means an entity that after the date of enactment of this Act directly (and not exclusively through any affiliate):

  • New drug means: (i) any drug, except a new animal drug or an animal feed bearing or containing

  • medicinal product means any substance or combination of substances presented for treating or preventing disease in human beings or animals and any substance or combination of substances which may be administered to human beings or animals with a view to making a medical diagnosis or to restoring, correcting or modifying physiological functions in humans or in animals;