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

  • 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.

  • 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.

  • 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).

  • 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 for industry Submission Documentation for Sterilization Process Validation in Applications for Human and Veterinary Drug Products).

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

  • 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.

  • This policy is based on the following key principles:- That adult safeguarding work should be based on the following principles:- • No abuse is acceptable.

  • The National Veterinary Drug Residue Monitoring Program was created by virtue of DA Administrative Order No. 14 s.


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 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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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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Related to Veterinary Drug

  • veterinary clinic means a building where animals are given medication or surgical treatment and are cared for during the time of such treatment for financial gain;

  • 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.

  • Active Pharmaceutical Ingredient or “API” means the active pharmaceutical substance of the Drug in bulk form prior to incorporation into the Product.

  • Automated drug dispensing system means a mechanical or electronic system that performs

  • 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.

  • Therapeutic interchange means an authorized exchange of therapeutic alternate drug products in accordance with a previously established and approved written protocol.

  • Radiopharmaceutical quality assurance means, but is not limited to, the performance of appropriate chemical, biological, and physical tests on potential radiopharmaceuticals and the interpretation of the resulting data to determine their suitability for use in humans and animals, including internal test assessment, authentication of product history, and the keeping of proper records.

  • 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):

  • Analytical x-ray system means a group of components utilizing x-rays to determine the elemental composition or to examine the microstructure of materials.

  • Radiopharmaceutical service means, but is not limited to, the procurement, storage, handling preparation, labeling, quality assurance testing, dispensing, delivery, recordkeeping, and disposal of radiopharmaceuticals and other drugs.

  • Bulk drug substance means any substance that is represented for use, and that, when used in the

  • Specialty drug means a prescription drug that:

  • 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;

  • Biological Samples means any physical samples obtained from Study Participants in accordance with the Protocol for the purposes of the Study.

  • Diagnostic x-ray system means an x-ray system designed for irradiation of any part of the human or animal body for the purpose of diagnosis or visualization.

  • Biological safety cabinet means a containment unit suitable for the preparation of low to moderate risk agents where there is a need for protection of the product, personnel, and environment, according to National Sanitation Foundation (NSF) Standard 49.

  • Therapeutic care means services provided by licensed or certified speech pathologists, Occupational Therapists and Physical Therapists.

  • Investigational Medicinal Product means the study drug or control material as defined in the Protocol.

  • Diagnostic source assembly means the tube housing assembly with a beam-limiting device attached.

  • cGMP means current Good Manufacturing Practices as specified in the United States Code of Federal Regulations, ICH Guideline Q7A, or equivalent laws, rules, or regulations of an applicable Regulatory Authority at the time of manufacture.

  • Therapeutic school means a residential group living facility:

  • Medical marijuana waste or "waste" means unused,