Chemical Ingredients definition

Chemical Ingredients means paclitaxel and albumin. --------------------
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Chemical Ingredients means, with respect to the Product or any Pipeline Product, the active pharmaceutical ingredient(s) and human albumin in the Product or Pipeline Product, as applicable.
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Examples of Chemical Ingredients in a sentence

  • The Specialty Chemical Ingredients (SCI) Initiative is pleased to spotlight BioAlberta – the Association for Life Sciences Industry.

  • In addition, students shall be classified as a chronic truant if the student is absent from school without a valid excuse for ten (10) percent or more of the school days in one school year, from the date of enrollment to the current date.

  • This would require additional work to validate assumptions used in the exposure criteria.3) The Safer Chemical Ingredients List (SCIL)The EPA’s Safer Choice program’s Safer Chemical Ingredients List35 is a list of low hazard chemicals that could be a complement to any other organizing tool to identify chemicals for prioritization under TSCA.

  • A key purpose of the partnership program is to recognize and encourage the formulation of products with environmentally preferable chemistry and collateral benefits, as defined and described in the Safer Choice Standard and the associated Criteria for Safer Chemical Ingredients.

  • Background on SCIL The Safer Chemical Ingredients List (SCIL) is the EPA’s Safer Choice program’s listing of chemical ingredients that meet its low-concern criteria and are generally acceptable for use in Safer Choice-labeled products.

  • APP shall order, but ABI shall pay for, all Chemical Ingredients for Product for commercial sale by ABI Parties.

  • Ingredients on authoritative lists of chemicals prohibited or restricted for use in cosmetics—notably, the FDA Cosmetics list (see 21 CFR 700.11 et seq.), the European Union Cosmetic Directive (Annex II), the Health Canada “Hotlist,” and the Cosmetic Ingredient Review “Unsafe for Use” list (at http://www.cir- safety.org)—will not be acceptable in labeled products, as confirmed by their toxicological hazard and failure to pass the Criteria for Safer Chemical Ingredients.

  • Counts of products that are labeled safer and chemicals on the Safer Chemical Ingredients List do not provide evidence that consumers are actually purchasing and using these products instead of other products and, thus, having the desired pollution prevention and risk reduction impact.

  • A subset of the Safer Chemical Ingredients List (SCIL) chemicals (low-hazard, green circle) are an appropriate starting place for identifying potential low-priority chemicals.

  • To qualify as fragrance-free, a product must only contain ingredients on or eligible for the Agency’s Safer Chemical Ingredients List (SCIL)—the list of ingredients that meet the Safer Choice safer chemical criteria and are acceptable for use in labeled products.

Related to Chemical Ingredients

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

  • Inert ingredient means an ingredient which is not an active ingredient.

  • 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;

  • Active Ingredient means the clinically active material(s) that provide pharmacological activity in a pharmaceutical product (excluding formulation components such as coatings, stabilizers, excipients or solvents, adjuvants or controlled release technologies).

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

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

  • Manufacturing Know-How means, with respect to the Product or any Variant thereof, the technology, data, designs, processes, methods, specifications and other know-how used in connection with the formulation, manufacture, labeling, packaging, quality control, release testing, and production of the Product, and all ingredients used therein and portions thereof.

  • 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.

  • 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;

  • Compounds means any or all of the following chemicals, as the context requires:

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

  • Biological Material means any material containing genetic information and capable of reproducing itself or being reproduced in a biological system;

  • Biological Materials means certain tangible biological materials that are necessary for the effective exercise of the Patent Rights, which materials are described on Exhibit A, as well as tangible materials that are routinely produced through use of the original materials, including, for example, any progeny derived from a cell line, monoclonal antibodies produced by hybridoma cells, DNA or RNA replicated from isolated DNA or RNA, recombinant proteins produced through use of isolated DNA or RNA, and substances routinely purified from a source material included in the original materials (such as recombinant proteins isolated from a cell extract or supernatant by non-proprietary affinity purification methods). These Biological Materials shall be listed on Exhibit A, which will be periodically amended to include any additional Biological Materials that Medical School may furnish to Company.

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

  • Biological agent shall mean any pathogenic (disease producing) micro-organism(s) and/or biologically produced toxin(s) (including genetically modified organisms and chemically synthesized toxins) which cause illness and/or death in humans, animals or plants.

  • 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.

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

  • 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.

  • 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.”

  • Products means information resources technologies that are, or are related to, EIR.

  • Chemical agent shall mean any compound which, when suitably disseminated, produces incapacitating, damaging or lethal effects on people, animals, plants or material property.

  • Formulation means the combination of various ingredients designed to render the product useful and effective for the purpose claimed, or the form of pesticide as purchased by users;

  • Radionuclide means a radioactive element or a radioactive isotope.

  • Therapeutically equivalent drug products means drug products that contain the same active

  • Additives means non-hydrocarbon compounds added to or blended with a product to modify its properties;

  • Radioactive Products or Waste means any radioactive material produced in, or any material made radioactive by exposure to the radiation incidental to the production or utilisation of nuclear fuel, but does not include radioisotopes which have reached the final stage of fabrication so as to be usable for any scientific, medical, agricultural, commercial or industrial purpose.