Manufacturing Schedule definition

Manufacturing Schedule means the plan containing the schedule of manufacturing needs and timing for the delivery of each manufacturing run of the Bulk Drug Substance set forth on Exhibit A, as amended, supplemented or restated from time to time by mutual written agreement of the parties.
Manufacturing Schedule shall have the meaning set forth in Section 4.3.
Manufacturing Schedule. - means the schedule submitted by the Contractor and accepted by PN.

Examples of Manufacturing Schedule in a sentence

  • Each Manufacturing Schedule shall include the expected delivery dates by calendar quarters of the Batches ordered for the calendar year.

  • At least ten (10) days prior to the start date of manufacture of a Batch set forth in the applicable Manufacturing Schedule, Praecis shall furnish the Intermediate to Oread at the Facility, free of charge, in such quantities as are necessary to enable Oread to manufacture the quantities of Product set forth in the applicable Purchase Order for such month.

  • Manufacturing Schedule 2005 *** *** Confidential material redacted and submitted separately to the Commission EXHIBIT B: PURCHASE PRICE (COMMERCIAL AGREEMENT) OVERVIEW The manufacturing process will be in conformance with ICH Q7A guidelines and will meet Avid's internal policies and procedures for the manufacturing in a multi-product facility.

  • Subject to 2.2.5, HALOZYME recognizes that AVID will reserve certain manufacturing capacity for HALOZYME to meet the BDS requirements set forth in the Manufacturing Schedule.

  • Annexure-A Suggested structural arrangement of the cabinet (Sheet 1/4) ANNEXURE-C Delivery Schedule and Technical Data to be furnished by Bidder 1.0 Delivery and Manufacturing Schedule 1.1 Time in weeks after receipt of order1.2 Schedule of date for submitting drawings for approval.1.3 Completion of fabrication the panel.1.4 Completion of Seismic test and other tests 2.0 Technical Data:Dimensions of the Cabinet a) Lengthb) Depthc) HeightColor Shade no.

  • Any such amendment or change order request shall address the impact of such amendment or change order request on the Contract Price and Manufacturing Schedule and the Parties agree to make an equitable adjustment to the Contract Price and the time or schedule for performing or completing the Work in connection with each Contract Change.

  • HALOZYME will use commercially reasonable efforts to provide AVID with a 2006 Manufacturing Schedule by the end of the ***.

  • The period of performance of this task order shall be from October 1, 2020 through December 31, 2020.F.2 Deliverable RequirementsF.2.1 Manufacturing Schedule with Allocated Capacity through Period of PerformanceA Manufacturing Schedule shall be provided that includes the utilization and non-utilization of the reserved manufacturing capacities (Bayview [**] Drug Substance) for the entire period of performance.

  • Subject to 2.2.5 and 3.4.1(a), HALOZYME recognizes that AVID will reserve certain manufacturing capacity for HALOZYME to meet the BDS requirements set forth in the Manufacturing Schedule.

  • The first three months of such Manufacturing Schedule shall be firm and may not be altered without the written consent of Praecis.


More Definitions of Manufacturing Schedule

Manufacturing Schedule means the twelve-month rolling manufacturing schedule for the Product at the Facility prepared by Oread and delivered to Praecis in accordance with Section 5.2 hereof.
Manufacturing Schedule has the meaning set out in paragraph 25.1 (Manufacturing Schedule) of Schedule 3 (Milestones and Deliverables);
Manufacturing Schedule has the meaning ascribed in Section 3.2(a).
Manufacturing Schedule means an agreed upon schedule establishing the following material terms: (i) the minimum and maximum quarterly quantities of PRODUCTS which AAI is obligated to produce and PHARMAPRINT is obligated to purchase; (ii) the intended twelvemonth MANUFACTURING SCHEDULE of PRODUCT; and (iii) the minimum purchase order quality for PRODUCT. The MANUFACTURING SCHEDULE shall be attached hereto and incorporated as Exhibit "C". 1.12 "MINIMUM QUARTERLY FEE" shall mean the amount set forth on Exhibit "D" specifying the minimum dollar amount of PRODUCT PHARMAPRINT is committed to purchase in each CALENDAR QUARTER of this Agreement. 1.13 "PREPARATION", "PREPARED" and/or "PREPARE" shall mean any and all steps and operations required in the blending and/or encapsulation of the PRODUCTS. 1.14 "PRODUCT" and/or "PRODUCTS" shall mean one-or more of the nutritional compounds set forth on Exhibit "A" attached hereto, as may be amended, PREPARED in bulk according to the SPECIFICATIONS at the unit prices set forth therein. 1.15 "QUARTERLY SHORTFALL" shall mean the difference between the MINIMUM QUARTERLY FEE and the dollar amount of PRODUCTS purchased, less any AAI out-of-pocket savings for MANUFACTURING MATERIALS, during any CALENDAR QUARTER in which the MINIMUM QUARTERLY FEE exceeded the dollar amount of PRODUCTS purchased. 1.16 "SPECIFICATIONS" shall mean those blending, manufacturing, encapsulation, sampling, shipping, container, storage, etc. SPECIFICATIONS including, but not limited to, relevant notification provisions established and provided by PHARMAPRINT and agreed upon by AAI for each PRODUCT. Said SPECIFICATIONS shall be attached hereto as Exhibit "B".
Manufacturing Schedule. Manufacturing Schedule shall mean the [***] or [***] rolling schedule for Processing and/or Packaging of a specific Product at the Facility as prepared by Contractor and accepted by Allergan.

Related to Manufacturing Schedule

  • Manufacturing Services means the manufacturing, quality control, quality assurance, stability testing, packaging, and related services, as set forth in this Agreement, required to manufacture Product or Products using the Active Materials, Components, and Xxxx Back Items;

  • Manufacturing Site means the facilities where a Compound is Manufactured by or on behalf of a Party, as such Manufacturing Site may change from time to time in accordance with Section 8.7.

  • Product Specification means a product specification for a Medical Device set out in Schedule 2;

  • Product Schedule means the “Product Schedule” that forms part of the Contract.

  • Product Specifications means the specifications, features and/or terms of any "Contract" (as defined in the LME Rules) listed for trading on the LME, as described in the LME Rules;

  • Manufacturing Process means any process for—

  • Manufacturing Facility means buildings and structures, including machinery and equipment, the primary purpose of which is or will be the manufacture of tangible goods or materials or the processing of such goods or materials by physical or chemical change.

  • MSAA Indicator Technical Specifications document means, as the context requires, either or both of the document entitled “Multi-Sector Service Accountability Agreement (MSAA) 2019-20 Indicator Technical Specifications November 5, 2018 Version 1.3” and the document entitled “Multi-Sector Service Accountability Agreement (MSAA) 2019-20 Target and Corridor-Setting Guidelines” as they may be amended or replaced from time to time;

  • technical specification means a document that prescribes technical requirements to be fulfilled by a product, process or service;

  • 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.

  • Monitoring Schedule means the Schedule containing details of the monitoring arrangements.

  • Technical Specifications A specification in a document defining the characteristics of a product or a service, such as the quality levels, the environmental and climate performance levels, the design for all needs, including accessibility for people with disabilities, and the evaluation of conformity, of product performance, of the use of the product, safety or dimensions, as well as requirements applicable to the product as regards the name by which it is sold, terminology, symbols, testing and test methods, packaging, marking or labelling, instructions for use, the production processes and methods at every stage in the life cycle of the supply or service, as well as the evaluation and conformity procedures;

  • Contract Specifications means the principal trading terms in CFD (for example Spread, Swaps, Lot Size, Initial Margin, Necessary Margin, Hedged Margin, the minimum level for placing Stop Loss, Take Profit and Limit Orders, financing charges, charges etc) for each type of CFD as determined by the Company from time to time. The Contract Specifications appear on the Website.

  • Additional Product means any Product identified as such in the Product Terms and chosen by Enrolled Affiliate under this Enrollment.

  • 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.

  • Clinical Supply Agreement has the meaning set forth in Section 4.2.

  • Product Specific Terms means the terms applicable to a specific item of Licensed Software as set out in Schedule 2;

  • Service Specification means and include detailed description, statements to technical data, performance characteristics, and standards (Indian as well as) as applicable and as specified in the Contract as well as those specifications relating to Industry standards and codes applicable to the performance of the work, work performance quality and the specifications affecting the works or any additional specification required to be produced by the DCO to meet the design criteria.

  • Manufacturing Materials means parts, tools, dies, jigs, fixtures, plans, drawings, and information produced or acquired, or rights acquired, specifically to fulfill obligations set forth herein.

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

  • Quality Agreement has the meaning set forth in Section 9.6.

  • Service Specifications means the following documents, as applicable to the Services under Your order: (a) the Oracle Cloud Hosting and Delivery Policies, the Program Documentation, the Oracle service descriptions, and the Data Processing Agreement described in this Schedule C; (b) Oracle’s privacy policies; and (c) any other Oracle documents that are referenced in or incorporated into Your order. The following do not apply to any non-Cloud Oracle service offerings acquired in Your order, such as professional services: the Oracle Cloud Hosting and Delivery Policies, Program Documentation, and the Data Processing Agreement. The following do not apply to any Oracle Software: the Oracle Cloud Hosting and Delivery Policies, Oracle service descriptions, and the Data Processing Agreement.

  • Bulk Product means Licensed Product supplied in a form other than Finished Product which can be converted into Finished Product.

  • Drug sample means a unit of a prescription drug that is not intended to be sold and is intended to promote the sale of the drug.

  • Drug Product means a specific drug in dosage form from a known source of manufacture, whether

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