Chemical Ingredients definition

Chemical Ingredients means paclitaxel and albumin. --------------------
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.

Examples of Chemical Ingredients in a sentence

  • To the extent the batches of Rejected Product exceed such (***) or (***), as applicable, GENERICO shall reimburse NEW ALPHA for the Chemical Ingredients and Materials used in the New Alpha Manufacturing of such excess Rejected Product.

  • The DfE Safer Chemical Ingredients List meets the DfE Safer Chemical criteria and is used for DfE-labeled Products.

  • Innovations in Safer Chemistry and Other Efforts to Advance Safer Choice, Environmental Protection, and Environmental Justice Describe your efforts/successes in developing safer chemicals for use in Safer Choice-certified products (include number of chemicals listed on the Safer Chemical Ingredients List (SCIL) or, CleanGredients database or used in Safer Choice-certified products).

  • APP will be entitled at any time during the Term to increase the Non-Commercial Price to account for increases, and shall decrease the Non-Commercial Price to account for decreases, (which must be reasonably documented by APP to ABI) in the cost of Chemical Ingredients.

  • APP will exclusively order and purchase all Chemical Ingredients used by APP to manufacture the Product for itself or for the ABI Parties from those sources.

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

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

  • Petition to Request Health and Environmental Testing and Regulation on Polyvinyl Alcohol Under the Toxic Substances Control Act and an Update to the Chemical Safety Status of Polyvinyl Alcohol on the EPA’s Safer Chemical Ingredients Lists.

  • 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.

  • The petition also requests under the Administrative Procedure Act (APA) that EPA update the status of PVA on EPA’s Safer Chemical Ingredients List (SCIL) from ‘‘green circle’’ to ‘‘gray square’’ until the testing is complete and reviewed by EPA.

Related to Chemical Ingredients

  • 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”).

  • 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;

  • Feed ingredient means each of the constituent materials making up a commercial feed.

  • 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 all information, techniques, inventions, discoveries, improvements, practices, methods, knowledge, skill, experience and other technology, whether or not patentable or copyrightable, and any copyrights based thereon, relating to or necessary or useful for the production, purification, packaging, storage and transportation of Collaboration Products, including without limitation specifications, acceptance criteria, manufacturing batch records, standard operating procedures, engineering plans, installation, operation and process qualification protocols for equipment, validation records, master files submitted to the FDA, process validation reports, environmental monitoring processes, test data including pharmacological, toxicological and clinical test data, cost data and employee training materials.

  • 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 ingredients and are identical in strength or concentration, dosage form, and route of administration and that are classified as being therapeutically equivalent by the U.S. Food and Drug Administration pursuant to the definition of "therapeutically equivalent drug products" set forth in the most recent edition of the Approved Drug Products with Therapeutic Equivalence Evaluations, otherwise known as the "Orange Book."

  • 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.