Pharmaceutical grade definition

Pharmaceutical grade means medical cannabidiol that meets standards for content, contamination, and consistency set by the department as determined by testing conducted at a laboratory pursuant to Iowa Code chapter 124E and these rules.
Pharmaceutical grade. (1) Saw Palmetto, (2) St. John's Wort, (3) Echinacea, (4) Valerian, (5) Ginseng, (6) Black Cohosh, (7) Agnus Castus, (8) Garlic, (9) Ginkgo Biloba, (10) Bilberry, and (11) Milk Thistle" (the "SPECIFIC APPLICATIONS") (the Broad Process Application and the Specific Applications referred to herein as the "P&E Filed Applications") (i) have been properly prepared and filed in a timely manner so as to obtain the benefit of any priority claimed from previously filed United States patent applications, and (ii) include all information and disclosures required under applicable law and regulations, and all of the Applications are being diligently pursued by the Company.

Examples of Pharmaceutical grade in a sentence

  • Pharmaceutical grade versions are not available in the United States and thus, these medications are not recommended.

  • Pharmaceutical grade drugs will have a National Drug Code (an NDC) that can be found on the packaging.

  • Iron and Folic acid Syrup shall be packed in 50 ml capacity Pharmaceutical grade polyethylene terephthalate amber coloured bottles (AA8011 / AA 1200); and provided with temper evident ROPP cap (25/15mm or 25/17mm).

  • Upon completion of the transaction, the Company carries on the business of EXM Holdings which is to plan to operate cannabis and hemp farms and a Pharmaceutical grade refining facility in Portugal to produce cannabinoid ingredients for the international market.

  • Pharmaceutical grade drugs are formulated to a standard compatible with the legal and ethical treatment of human or veterinary patients in a health care or practice setting by a pharmaceutical company or qualified compounding pharmacist.

  • Pharmaceutical grade is strongly recommended.🞎 Thermometer Guide and Temperature Monitoring Guidelines: Must have digital data loggers or continuous monitoring systems.

  • Figure 5: SEM images showing details of particle surface of different washing grade lac- tose powders: (A) Wash 0; (B) Wash 0.5; (C) Wash 1; (D) Wash 2; (E) Pharmaceutical grade lactose.

  • Pharmaceutical grade allergen extracts are expected to show similar qualitative binding using immunoblots as well as variation in total IgE binding between 50% and 150% of the extract standard mean serum IgE binding using pooled allergic sera to compare one batch of allergen extract to a previous batch[93,95].

  • Describe the issuers’ principal products or services, and their markets The Company’s principal activities will now be through BioCann Pharma S.A.S. which is engaged in the sourcing of Marijuana crop in Colombia from Licensed Growers and the processing of Pharmaceutical grade CBD Oils through a Joint Venture with a Licensed Processor in the Republic of Colombia.

  • Pharmaceutical grade excipients were obtained from Pharmaceutical Technology Lab.

Related to Pharmaceutical grade

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

  • 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.

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

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

  • 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.

  • Pharmaceutical care means the provision of drug therapy and

  • 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.

  • Generic means that no specific brand or name shall be included as part of the specifications unless such a brand or name is required to identify the intent of a purchase, order or proposal.

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

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

  • 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.

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

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

  • 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.

  • 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.

  • Successor manufacturer means a manufacturer that acquires, succeeds to, or assumes any part of the business of another manufacturer as the result of any of the following:

  • Generic Product means any pharmaceutical product that (i) is sold by a Third Party that is not an Affiliate or licensee of Buyer and (ii) (a) contains the same active pharmaceutical ingredient as the Product or (b) is categorized by the applicable Governmental Entity in a country to be therapeutically equivalent to, or interchangeable with, the Product, such that the pharmaceutical product may be substituted for the Product at the point of dispensing without any intervention by the prescribing physician in such country.

  • Therapeutic school means a residential group living facility:

  • ingredient means any substance, including a food additive used in the manufacture or preparation of food and present in the final product, possibly in a modified form;

  • Drug outlet means a pharmacy, nursing home, shelter home, convalescent home, extended care facility, drug abuse treatment center, penal institution, hospital, family planning clinic, student health center, retail store, wholesaler, manufacturer, mail-order vendor or other establishment with facilities located within or out of this state that is engaged in dispensing, delivery or distribution of drugs within this state.

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

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

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

  • Least developed country end product means an article that—

  • 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;

  • 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.