Pharmaceutical Drug definition

Pharmaceutical Drug means a synthetic or natural chemical recognised by any official regulatory body in the appropriate jurisdiction:
Pharmaceutical Drug means a drug intended for use in preventing or curing disease or relieving pain.
Pharmaceutical Drug. (also referred to as medicine, medication, or simply as drug) is a drug used to diagnose, cure, treat, or prevent disease.

Examples of Pharmaceutical Drug in a sentence

  • The Distributor is obliged to ensure the compliance of Anti-Unfair Competition Law, Laws on the Advertising and Marketing of Pharmaceutical Drug Products, the Securities Act of the United States and any other applicable laws and regulations for all and any of its publicity and advertising activities.

  • Clinical Trialsmeans an organised study or test undertaken that uses human Research Subjects to establish the effectiveness, bioequivalence or safety of a Pharmaceutical Drug, Bio Science Product and/or Medical Device, under proper conditions of use and shall include any pre-trial assessment.

  • The four programmes are the two- year Master programme in Medical and Pharmaceutical Drug Innovation at the Rijksuniversiteit Groningen, the one-year Master programme in Translational Medical Research at Xxxxxxxx-Xxxxx-Universität Heidelberg, and the two-year Master programmes in Molecular Medicine and Medical Research at Uppsala Universitet.

  • Occurrence and Environmental Behavior of the Chiral Pharmaceutical Drug Ibuprofen in Surface Waters and in Wastewater.

  • This resulted in 331 terms for Medical Finding, 278 for Pharmaceutical Drug and 214 for Body Part.The sets of terms were divided into two equally large groups, group A and group B.

  • REGULAR CALENDAR, CONTINUED GENERAL GOVERNMENT ADMINISTRATIVE OFFICE/BOARD OF SUPERVISORS LEGISLATIVE UPDATE/SUPERVISORS’ REPORTS County Executive Officer (CEO) Larry Lees presented an update on specific legislation of importance to Shasta County, including Senate Bill 212 (Jackson and Ting), Sharps and Pharmaceutical Drug Take-Back Program.

  • Standard pre-processing and total lem- matisation produced similar results for all three semantic categories, which shows that retaining some of the inflected information does not con- tribute to the term extraction.Retaining case particles for Medical Finding and Pharmaceutical Drug produced low results, re- gardless of window size.

  • Noted are the following compliance issues:The Company uses a combination of internal and external distribution methodologies for the Medco Pharmaceutical Drug Plan.

  • Exclusion of Objectionable Microorganisms from Non‐sterile Pharmaceutical Drug Products.

  • Kos will maintain records as required by the Pharmaceutical Drug Marketing Act and all other applicable laws and will allow representatives of Jerini to inspect such records during Kos’s regular business hours, upon reasonable advance written request and subject to Jerini’s obligations set forth in Section 12 herein; provided, that Jerini will be permitted only * * * such inspection during any * * * period.


More Definitions of Pharmaceutical Drug

Pharmaceutical Drug means any product sold for human medical or veterinary use,

Related to Pharmaceutical Drug

  • Pharmaceutical Product shall have the meaning ascribed to such term in Section 3.1(hh).

  • Active Pharmaceutical Ingredient or “API” shall mean one or more of the following active pharmaceutical ingredients: tenofovir alafenamide (“TAF”), tenofovir disoproxil fumarate (“TDF”), elvitegravir (“EVG”), and cobicistat (“COBI”).

  • Radiopharmaceutical means any drug that exhibits spontaneous disintegration of unstable nuclei with the emission of nuclear particles or photons and includes any non-radioactive reagent kit or radionuclide generator that is intended to be used in the preparation of any such substance, but does not include drugs such as carbon-containing compounds or potassium-containing salts that include trace quantities of naturally occurring radionuclides. The term also includes any biological product that is labeled with a radionuclide or intended solely to be labeled with a radionuclide.

  • Pharmaceutical care means the provision of drug therapy and

  • 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.

  • 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.

  • 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;

  • Therapeutic diet means meals served that are soft, low-fat, low-sodium or controlled calorie.

  • 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 a Prescription Drug that is medically equivalent to a Brand Name Drug as determined by the FDA. It meets the same standards as a Brand Name Drug for purity, safety, strength and effectiveness and is manufactured and sold under its chemical, common, or official name.

  • Therapeutic Product means a health product categorised as a therapeutic product in the First Schedule to the Act;

  • in vitro diagnostic medical device means any medical device which is a reagent, reagent product, calibrator, control material, kit, instrument, apparatus, equipment, software or system, whether used alone or in combination, intended by the manufacturer to be used in vitro for the examination of specimens, including blood and tissue donations, derived from the human body, solely or principally for the purpose of providing information:

  • Marihuana-infused product means a topical formulation, tincture, beverage, edible substance, or similar product containing marihuana and other ingredients and that is intended for human consumption.

  • Therapeutic school means a residential group living facility:

  • Biological product means a virus, therapeutic serum, toxin, antitoxin, vaccine, blood, blood component or derivative, allergenic product, protein other than a chemically synthesized polypeptide, or analogous product, or arsphenamine or any derivative of arsphenamine or any other trivalent organic arsenic compound, applicable to the prevention, treatment, or cure of a disease or condition of human beings.

  • Drug means (i) articles or substances recognized in the official United States Pharmacopoeia

  • Biosimilar Product means, with respect to a Licensed Product and on a country-by-country basis, a product that [***].

  • Biologics License Application or “BLA” means an application requesting permission from the FDA to introduce, or deliver for introduction, a biological product into interstate commerce, or any similar application or submission for marketing authorization of a product filed with a Regulatory Authority to obtain Regulatory Approval for such product in a country or group of countries.

  • Collaborative drug therapy management means participation by an authorized pharmacist and a physician in the management of drug therapy pursuant to a written community practice protocol or a written hospital practice protocol.

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

  • Drug abuse means any pattern of pathological use of drugs that causes impairment in social or occupational functioning, or that produces physiological dependency evidenced by physical tolerance or by physical symptoms when it is withdrawn.

  • Reference biological product means the single biological product licensed pursuant to 42 U.S.C.

  • Drug addiction means a disease characterized by a

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

  • Biological diversity means the variability among living organisms from all sources including, inter alia, terrestrial, marine and other aquatic ecosystems and the ecological complexes of which they are part; this includes diversity within species, between species and of ecosystems.

  • FDA means the United States Food and Drug Administration and any successor agency thereto.