We use cookies on our site to analyze traffic, enhance your experience, and provide you with tailored content.

For more information visit our privacy policy.

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. 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")

Examples of Pharmaceutical grade in a sentence

  • 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).

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

  • 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.

  • 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 VDG, certified to contain 99.6% and Galvus® tablets (batch no: S0421A), nominally containing 50 mg VDG per tablet, were kindly supplied from Novartis Pharma AG Co. (Basle, Switzerland).A solution of 0.5% (w/v) of 1,2-naphthoquinone-4-sulfonic acid sodium salt (NQS; Hopkin and Williams, Chadwell Health, Essex, England) was prepared by dissolving 250 mg in 50 mL distilled water.

  • Pharmaceutical grade saxagliptin hydrochloride, certified to contain 99.8% and Onglyza® tablets (batch no: 1E6034B), nominally containing 5.58 mg anhydrous saxagliptin hydro- chloride equivalent to 5 mg SAX per tablet, were kindly sup- plied from Bristol-Myers Squibb Company (Indiana, USA).

  • Pharmaceutical grade (Pharmed) tubing should be used for the section around the rotor head of a peristaltic pump, to minimize gaseous diffusion.

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

  • Pharmaceutical grade castor oil (CO; MW = 934 g·mol-1) was purchased from Cooper Pharmaceutique.

  • It is interesting to note the lack of interest shown by the ESB Group of unions in general, regarding the issue of gender balance and worker directors in the ESB.

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

  • 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) meets 1 or more of the following:

  • 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.

  • Approved Product means any water fitting, plumbing product, material or component which is the subject of an existing WRAS Approval;