Contract Requirements means ************************* of Lilly's requirements for Bulk Drug Substance. Lilly may at its option commence a commercial scale process development project for the Bulk Drug Substance to enable Lilly to register its facilities or those of a Third Party contingent manufacturer in the registration. Lilly or the Third Party may manufacture limited quantities of the Bulk Drug Substance as part of that development project. Lilly shall have the right to make and sell Drug Product made from limited quantities of Bulk Drug Substance that Lilly or its Third Party manufacturers have produced, in jurisdictions other than Major Markets. Lilly shall pay Ophidian a ************** on Net Sales of such limited quantities and Ophidian reserves the right to be the sole supplier of any of the materials, including but not limited to ************, used in the facility. Ophidian's Technology and Ophidian's Program Technology shall not be used in the contingent facilities to manufacture any substance other than the Bulk Drug Substance. Ophidian shall have the right to have a representative on site and audit these facilities at reasonable intervals upon reasonable notice.
Contract Requirements means one hundred percent (100%) of Lilly's requirements for Bulk Drug Substance.
Contract Requirements means all definitions, descriptions, requirements, criteria and performance standards relating to the Software which are set forth or referenced in: (a) the matrix attached as
Examples of Contract Requirements in a sentence
A sample shall be subjected to first article (FA) or product demonstration model (PDM) inspection as applicable, in accordance with the tests and inspections of Section E of this Performance-based Contract Requirements (PCR) document.
In addition to the specifications for the Project, the attached Appendices include the City’s Contract Requirements.
The finished product shall be examined for compliance with the performance requirements specified in Section C of this Performance-based Contract Requirements document utilizing the double sampling plans indicated in ANSI/ASQ Z1.4. The lot size shall be expressed in pouches.
Include but are not limited to, the Invitation for Bid, Instructions to Bidders, General Conditions, Special Conditions, Contract Requirements and Bid Forms/Attachments, Exhibits, Specifications/Special Provisions and Drawings, Pricing Response Form, and any Addenda issued prior to the date designated for receipt of Bids, as applicable.
Special Contract Requirements paragraph H047, Travel (FEB 2003) pertains to travel related to cost or labor hour CLIN's only.
More Definitions of Contract Requirements
Contract Requirements means PRAECIS' requirements for the development, and launch of Product in the United States and all other parts of the world during the term.
Contract Requirements means one hundred percent (100%) of the quantity of a Device used, sold and/or distributed by PURCHASER in the Territory.
Contract Requirements means one hundred percent (100%) of the worldwide commercial requirements for Drug Substance of Schein and its Affiliates.
Contract Requirements. The Project requirements specified in the Project Development Plan.
Contract Requirements means 100% of the quantity of a Device or Demo Device used, sold and/or distributed by Axogen in the Territory. 1.8 “Contract Price” shall mean the price paid by Axogen to CBI for each Device or Demo Device that is finished, packaged, labeled, and ready for subsequent sale, distribution, or other use (i.e., Demo Device(s)) by Axogen referenced in Exhibit B and as may be amended by the Parties from time to time. 1.9 “Current Good Manufacturing Practices” or “cGMP” shall mean the good manufacturing practices required by the FDA and set forth in the FD&C Act or FDA Regulations (including without limitation 21 CFR 820), policies or guidelines, in effect at any time during the term of this Agreement, for the manufacture of Devices. 1.10 “Delivery Date” shall mean the date that the Device is delivered to a common carrier chosen by CBI. 1.11 “Demo Device(s)” shall mean a version of the Device prepared for Axogen by CBI intended solely for demonstration that is manufactured or processed in the same manner as a Device; however, it will be: (i) non-sterile; (ii) not cleared for clinical, human use; and (iii) marked “NOT FOR CLINICAL USE.” 1.12 “Device(s)” shall mean the Base Component Material coated on both sides with HA+ Material including but not limited to that which is 4-layer Base Component Material and which is then supplied sterile to Axogen in sterile barrier packaging, product labeling, and outer product carton as set forth on Exhibit “A”. 1.13 “Existing Distribution Agreement” shall mean the Distribution Agreement between Axogen and CBI dated August 27, 2008, as amended, pursuant to which CBI granted to Axogen the exclusive worldwide right to market, sell and distribute certain products utilizing ECM and SIS technology in the “Field” as such term is defined therein currently marketed and sold under Axogen’s Axoguard® family of trademarks DocuSign Envelope ID: 4753CEFB-DE1B-430A-AE53-AD234F582049
Contract Requirements means the requirements of the Contract specified in Order Form.
Contract Requirements means one hundred percent (100%) of the worldwide requirements for Drug Substance of Steris and its Affiliates. 1.4 "Drug Substance" shall mean iron dextran bulk solution, as more fully described in the Drug Substance Specifications, as defined below.