Drug samples definition

Drug samples means any federal food and drug administration
Sample 1Sample 2Sample 3
Drug samples means any federal food and drug administration approved controlled substance, legend drug, or products requiring prescriptions in this state, which is distributed at no charge to a practitioner by a manufacturer or a manufacturer's representative, exclusive of drugs under clinical investigations approved by the federal food and drug administration.
Sample 1Sample 2

Examples of Drug samples in a sentence

  • Drug samples, which failed in the first analysis are sent to Government Analyst (GA).

  • Drug samples are forbidden in public health facilities unless a written district procedure approved by the State Office of Pharmacy has been established for their use by a licensed physician and a licensed pharmacist.

  • Levine’s study combines analysis of government and Church programs with interviews from the hierarchy to produce a balance between elite and popular viewpoints.

  • In the case of all disputes arising from the contractual relationship, if the advertiser is a businessman, a lawsuit must be brought to the court that is responsible for the headquarters of Actaria.

  • Drug samples collected throughout Spain can be sent to this facility.

  • Drug samples will be accepted as long as the label is clearly exposed.

  • Drug samples were drawn and sent to Guwahati for testing which took on an average of six months for analysis and receipt of test reports.

  • Drug samples for individual patient treatment may not be accepted from Vendors (see Pharmaceutical Services Department policy 3.09); this prohibition does not apply to drug samples or free drug used in the context of a clinical trial.

  • Drug samples are not permitted on the premises at NYP in Article 28 facilities and offices (See Hospital Policies and Procedures Manual: Drug Samples).

  • Drug samples also taken at a later time returned negative results to the presence of prohibited substances.

Related to Drug samples

  • Drug sample means a unit of a prescription drug that is not intended to be sold and is intended to promote the sale of the drug.

  • API means American Petroleum Institute.

  • Drug Substance means an active ingredient that is intended to furnish pharmacological activity or other direct effect in the diagnosis, cure, mitigation, treatment, or prevention of disease or to affect the structure or any function of the human body, but does not include intermediates used in the synthesis of such ingredient.

  • Finished Product means a cannabis product in its final form to be sold at a retail premises.

  • Drug Product means a specific drug in dosage form from a known source of manufacture, whether

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

  • Bulk Product means Licensed Product supplied in a form other than Finished Product which can be converted into Finished Product.

  • Product means any deliverable under the Contract, which may include commodities, services, technology or software.

  • Product Manufacturer means the entity that assembles the component parts to manufacture the final Product;

  • Hemp product means the same as that term is defined in § 3.2-4112.

  • Manufacturing Site means a location where a manufacturing

  • Manufacturing Process means any process for—

  • Finished Products means any one or more of the following petroleum oils, or a mixture or combination of these oils, to be used without further processing except blending by mechanical means:

  • Aerosol coating product means a pressurized coating product containing pigments or resins that dispenses product ingredients by means of a propellant, and is packaged in a disposable can for hand-held application, or for use in specialized equipment for ground traffic/marking applications.

  • Batch means a specific quantity of Product that is intended to have uniform character and quality, within specified limits, and is produced according to a single manufacturing order during the same cycle of manufacture.

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

  • Product Specifications means the specifications, features and/or terms of any "Contract" (as defined in the LME Rules) listed for trading on the LME, as described in the LME Rules;

  • Assay means a laboratory analysis of Crude Petroleum to include the following: A.P.I. Gravity, Reid vapor pressure, composition, pour point, water and sediment content, sulfur content, viscosity, distillation, hydrogen sulfide, flash/boiling point and other characteristics as may be required by Carrier.

  • Samples mean representative physical examples of materials, equipment or workmanship, used to confirm compliance with requirements and/or to establish standards for use in execution of the Work.

  • Non-Microsoft Product means any third-party-branded software, data, service, website or product, unless incorporated by Microsoft in a Product.

  • Milk product or "dairy product" means cottage cheese, dry curd cottage cheese, reduced fat cottage cheese, lowfat cottage cheese, cream, light cream, light whipping cream, heavy cream, heavy whipping cream, whipped cream, whipped light cream, sour cream, acidified sour cream, cultured sour cream, half-and-half, sour half-and-half, acidified sour half-and-half, cultured sour half-and-half, reconstituted or recombined milk and milk products, concentrated milk, concentrated milk products, skim milk, lowfat milk, frozen milk concentrate, flavored milk, eggnog, buttermilk, cultured milk, cultured lowfat milk, cultured skim milk, yogurt, lowfat yogurt, nonfat yogurt, acidified milk, acidified lowfat milk, acidified skim milk, low-sodium milk, low-sodium lowfat milk, low-sodium skim milk, lactose-reduced milk, lactose-reduced lowfat milk, lactose-reduced skim milk, aseptically processed and packaged milk, milk products with added safe and suitable microbial organisms, and any other milk product made by the addition or subtraction of milkfat or addition of safe and suitable optional ingredients for protein, vitamin, or mineral fortification. Unless a product is considered a milk product under this subdivision, milk product does not include dietary products, infant formula, ice cream or other desserts, cheese, or butter. Milk products include the following:

  • Manufactured end product means any end product in product and service codes (PSCs) 1000-9999, except—

  • Aerosol product means a pressurized spray system that dispenses product ingredients by means of a propellant contained in a product or a product's container, or by means of a mechanically induced force. “Aerosol Product” does not include “Pump Spray.”

  • Contract Manufacturer means a company that produces goods under contract for another company under the label or brand name of that company.

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

  • Active Ingredient means any com- ponent that is intended to furnish pharmacological activity or other di- rect effect in the diagnosis, cure, miti- gation, treatment, or prevention of dis- ease, or to affect the structure or any function of the body of humans. The term includes those components that may undergo chemical change in the manufacture of the drug product and be present in the drug product in a modified form intended to furnish the specified activity or effect.