Processed Tissues definition

Processed Tissues means xenograft and allograft bone tissue ----------------- processed by Tutogen or an Affiliate of Tutogen or a Permitted Successor of Tutogen, as listed in Schedule A attached hereto. The parties shall mutually agree as to the addition of processed tissues to Schedule A. To the extent that a Processed Tissue is not available from Tutogen at the time of its listing on Schedule A, the parties agree to collaborate on its final design and development in accordance with Sections 2 and 3 of the First Amended Processed Tissue Development and License Agreement of even date between Sulzer and an Affiliate of Tutogen.
Processed Tissues means all xenograft and allograft bone ----------------- tissues processed by Tutogen or an Affiliate of Tutogen or a Permitted Successor of Tutogen for use in and adjoining the human maxilla or the human mandible.
Processed Tissues means the xenograft and allograft bone ----------------- tissues processed by Tutogen, as listed in Schedule A, as amended from time to time.

Examples of Processed Tissues in a sentence

  • The parties acknowledge that by reason of their --------------- relationship hereunder, each has had and will continue to have access to certain information and materials concerning the other's business, plans, customers, technology, and/or Processed Tissues that is considered by a party to be confidential ("Confidential Information") and of substantial value to that party, which value would be impaired if such information were disclosed to third parties.

  • In the event that Sulzer shall terminate this Agreement without cause as provided in this Section 7.4, neither Sulzer nor any Affiliate of Sulzer shall for a period of one year following the effective date of termination enter into an agreement, either directly or indirectly, to own, operate, advise, or have any interest in any business relating to the Processed Tissues in the Territory for the Field of Use.

  • In no event shall Sulzer acquire title to the consigned Processed Tissues.

  • Tutogen hereby grants Sulzer the exclusive right during --------------- the term of this Agreement to provide the Services for the Processed Tissues in the Territory for the Field of Use.

  • Notwithstanding the Force Majeure ---------------------------------- provision in Section 9.2, in the event that Tutogen is unable to supply Processed Tissues for a continuous period of six months because Tutogen, for whatever reason, is unable to obtain tissue donors, Sulzer shall have the right to terminate this Agreement.

  • Tutogen has disclosed to Sulzer all patents and other intellectual property rights which, to Tutogen's knowledge, may have a material effect on Sulzer's ability to make available the Processed Tissues.

  • Tutogen agrees to comply with and maintain compliance ----------------- with all governmental rules, regulations, statutes and other laws of any kind necessary to import into and distribute the Processed Tissues within the Territory.

  • Commencing with the second calendar quarter of 2001 and continuing quarterly thereafter, Sulzer shall provide Tutogen, no later than 15 days prior to each calendar quarter, with a rolling monthly forecast of demand for the Processed Tissues for the succeeding 12 months.

  • Within 30 days following execution of this Agreement, Sulzer ----------- shall provide Tutogen with a monthly forecast of demand for the Processed Tissues during the succeeding six-month period.

  • Sulzer shall incur no liability to Tutogen in the event that actual demand for the Processed Tissues differs from Sulzer's forecasts.


More Definitions of Processed Tissues

Processed Tissues means those tissue groups which have been (i) properly notified to Biocompatibles pursuant to Section 6.1 of the Research Agreement for license under this Agreement and (ii) treated with the Biocompatibles Technology. The parties shall endeavor to maintain a record of Processed Tissues by amending Schedule B attached hereto to include all tissue groups notified for inclusion as and when Biocompatibles receives proper notification.

Related to Processed Tissues

  • Goods/Materials means any of the articles, materials, machinery, equipments, supplies, drawing, data and other property and all services including but not limited to design, delivery, installation, inspection, testing and commissioning specified or required to complete the order.

  • 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.

  • Reagent means any product other than fuel that is stored on-board the vehicle and is provided to the exhaust after-treatment system upon request of the emission control system.

  • Raw Materials means all raw materials, supplies, components and packaging necessary to manufacture and ship the Product in accordance with the Specifications, as provided in Exhibit A, but not including the API.

  • API means the American Petroleum Institute.

  • Samples mean representative physical examples of materials, equipment or workmanship, used to confirm compliance with requirements and/or to establish standards for use in execution of the Work.

  • Finished Products means any one or more of the following petroleum oils, or a mixture or combination of these oils, to be used without further processing except blending by mechanical means:

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

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

  • Cost of materials means the cost of components, parts or materials which are intended for the production, manufacturing or assembling of the goods bid for and which are not produced, manufactured or assembled in the factory where the production, manufacture or assembly of such goods occurs, including freight, landing costs, port charges, import duties and other import costs of such components, parts or materials and all costs in connection with the handling and transport thereof prior to delivery at that factory;

  • Finished Goods means units of a manufactured product awaiting sale.

  • Manufacturing Process means any process for—

  • Labeling means all labels and other written, printed, or graphic matter on an article or any of its

  • Processes “Processing,” “Processed” means any operation or set of operations which is performed on data or sets of data, whether or not by automated means, such as collection, recording, organization, structuring, storage, adaptation or alteration, retrieval, consultation, use, disclosure by transmission, dissemination, or otherwise making available, alignment or combination, restriction, erasure, or destruction.

  • Hemp products means all products made from industrial hemp,

  • APIs means SAP application programming interface and accompanying or related Documentation, source code, tools, executable applications, libraries, subroutines, widgets and other materials made available by SAP or through SAP tools or SAP Software Development Kit (and all derivative works or modifications thereof) to Provider that allow Provider to integrate the Provider Service with the Cloud Service, including any access code, authentication keys or similar mechanisms to enable access of the APIs.

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

  • Manufacturing means all activities related to the manufacture of a Compound, including planning, purchasing, manufacture, processing, compounding, storage, filling, packaging, waste disposal, labeling, leafleting, testing, quality assurance, sample retention, stability testing, release, dispatch and supply, as applicable.

  • labelling means any words, particulars, trade marks, brand name, pictorial matter or symbol relating to a food and placed on any packaging, document, notice, label, ring or collar accompanying or referring to such food;

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

  • Product Labeling means, with respect to a Licensed Product in a country or other jurisdiction in the Territory, (a) the Regulatory Authority‑approved full prescribing information for such Licensed Product for such country or other jurisdiction, including any required patient information, and (b) all labels and other written, printed, or graphic matter upon a container, wrapper, or any package insert utilized with or for such Licensed Product in such country or other jurisdiction.

  • SAP Materials means any materials (including statistical reports) provided, developed or made available by SAP (independently or with Customer’s cooperation) in the course of performance under the Agreement, including in the delivery of any support or Professional Services to Customer. SAP Materials do not include the Customer Data, Customer Confidential Information or the Cloud Service. SAP Materials may also be referred to in the Agreement as “Cloud Materials”.

  • cGMP means current Good Manufacturing Practices as specified in the United States Code of Federal Regulations, ICH Guideline Q7A, or equivalent laws, rules, or regulations of an applicable Regulatory Authority at the time of manufacture.

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

  • Current Good Manufacturing Practices or “cGMP” means applicable Good Manufacturing Practices as specified in the United States Code of Federal Regulations and/or the EU Good Manufacturing Guidelines, and any successor legislation from time to time, prevailing at the time of the manufacture of the Product.

  • Recycled product means a product containing recovered material, or post-consumer recovered material, or both.