Prescription Pharmaceutical Product definition

Prescription Pharmaceutical Product means any pharmaceutical product with regulatory approval for any indication and in any galenic formulation that requires doctor's prescription in order to be sold to the consumers according to the national laws. For avoidance of doubt, OTC products are not Prescription Pharmaceutical Products. "Scope of the Agreement" shall mean HORMOS' rights to be licensed or materials to be transferred, as the case may be, related to HMRlignan(TM) as defined in this Agreement but consisting exhaustively of
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Prescription Pharmaceutical Product means any pharmaceutical or biological product (irrespective of patent status and/or whether it is branded or not), which is intended to be used in the prescription of or under the supervision of a Healthcare Professionals, and which is intended for use in the diagnosis, treatment or prevention of disease in humans, or to affect the structure or any function of the human body.
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Examples of Prescription Pharmaceutical Product in a sentence

  • Information to Supplement Package Inserts 1732.1 Outline of Prescription Pharmaceutical Product Information 1732.2 Pharmaceutical Interview Forms (IF) 1743.

  • Information to Supplement PackageInserts 1452.1 Outline of Prescription Pharmaceutical Product Information 1452.2 New Drug Approval Information Package (NAIP) 1462.3 Summary Basis of Reexamination (SBR) 1462.4 Pharmaceutical Interview Forms (IF)............................................................

  • Information to Supplement Package Insert 1772.1 Outline of Prescription Pharmaceutical Product Information 1772.2 Pharmaceutical Interview Forms (IF)·1783.

  • The JPMA provides certain rules on comparative advertisements of medic- inal products in the Guidelines for Preparation of Outline of Prescription Pharmaceutical Product Information.

  • Clause 36 applies to land adjoining or contiguous to land within Zone No 7(a).

  • Inserts 156 2.1 Outline of Prescription Pharmaceutical Product Information 156 2.2 New Drug Approval Information Package (NAIP) 156 2.3 Summary Basis of Reexamination (SBR) 156 2.4 Pharmaceutical Interview Forms (IF) .............................................................

  • Information to Supplement Package Inserts 139 2.1 Outline of Prescription Pharmaceutical Product Information 139 2.2 New Drug Approval Information Package (NAIP) 139 2.3 Summary Basis of Reexamination (SBR) 140 2.4 Pharmaceutical Interview Forms (IF) .............................................................

  • To ensure consistency of the content with that of the package insert, attention should be paid to the JPMA Code of Practice.In addition, the Outline of Prescription Pharmaceutical Product Information is internally reviewed by the pharmaceutical company and voluntarily reviewed by JPMA.

  • INFORMATION TO SUPPLEMENT PACKAGE INSERTS 942.1 Outline of Prescription Pharmaceutical Product Information2.2 Pharmaceutical Interview Forms (IF)3.

  • The Outline of Prescription Pharmaceutical Product Information is prepared by the manufacturing/marketing authorization holders with the objective of providing accurate and appropriate information to health professionals to promote proper use of their drugs.

Related to Prescription Pharmaceutical Product

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

  • 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.

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

  • 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;

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

  • Pharmaceutical means a drug intended for use in the diagnosis, cure, mitigation, treatment, therapy, or prevention of disease in humans or animals.

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

  • 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.”

  • 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.

  • Civil Aeronautical Product means any civil aircraft, aircraft engine, or propeller or subassembly, appliance, material, part, or component to be installed thereon.

  • Interchangeable biological product means a biological product that the U.S. Food and Drug Administration has:

  • 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.

  • 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.

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

  • 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.

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

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

  • 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.

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

  • Final Product means a product that is not used in producing other products and is built and intended for use outdoors, provided the final product has not deteriorated or has otherwise become a potential source of contaminants.

  • Tobacco product means any substance containing tobacco leaf, including but not limited to, cigarettes, cigars, pipe tobacco, hookah tobacco, snuff, chewing tobacco, dipping tobacco, bidis, blunts, clove cigarettes, or any other preparation of tobacco; and any product or formulation of matter containing biologically active amounts of nicotine that is manufactured, sold, offered for sale, or otherwise distributed with the expectation that the product or matter will be introduced into the human body by inhalation; but does not include any cessation product specifically approved by the U.S. Food and Drug Administration for use in treating nicotine or tobacco dependence.

  • Nicotine product means a product that contains nicotine and is not any of the following:

  • 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.

  • API means the American Petroleum Institute.

  • Marijuana product means marijuana as defined in 50-32-101 and marijuana-infused products

  • Finished Products means the fully assembled and shrink-wrapped Licensed Products, each including a Game Cartridge, Game Cartridge label and Printed Materials.