Manufacturing Transition Plan definition

Manufacturing Transition Plan means the manufacturing transition plan attached hereto as Exhibit C, which plan will include, among other things, terms relating to pricing, freight, cash discounts, volume rebates, credit terms and other material terms of sale.
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Manufacturing Transition Plan shall have the meaning assigned to it in Section 5.23.
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Manufacturing Transition Plan has the meaning set forth in Section 6.4.
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Examples of Manufacturing Transition Plan in a sentence

  • The Parties shall perform each activity allocated to such Party under the Manufacturing Transition ​ Plan and shall use Commercially Reasonable Efforts to implement the Manufacturing Technology Transfer to Gilead or its designee in accordance with the Manufacturing Transition Plan.


More Definitions of Manufacturing Transition Plan

Manufacturing Transition Plan shall have the meaning set forth in Section 2.6(b).
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Manufacturing Transition Plan has the meaning set forth in Section 8.11.2 (Manufacturing Transition Period).
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Manufacturing Transition Plan has the meaning set forth in Section 10.4 below.
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Manufacturing Transition Plan means the plan for the transfer of Licensed Technology, Regulatory Approvals and responsibilities for the Manufacture of Ridaforolimus from ARIAD to MERCK pursuant to the Manufacturing Transition Plan set forth in Schedule 6 attached hereto.
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Manufacturing Transition Plan is defined in Section 8.3 (Manufacturing Technology Transfer).
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Related to Manufacturing Transition Plan

  • Transition Plan means a transition plan, acceptable to the LHIN that indicates how the needs of the HSP’s clients will be met following the termination of this Agreement and how the transition of the clients to new service providers will be effected in a timely manner; and

  • Manufacturing Agreement has the meaning set forth in Section 4.3.

  • Commercialization Plan has the meaning set forth in Section 6.2.

  • Manufacturing Process means any process for—

  • Project Implementation Plan means the detail plan submitted by the Developer with regard to development of Project Facilities and its operation and management thereof in accordance with this Agreement and to be appended as Schedule 9 to this Agreement.

  • Development Plans has the meaning set forth in Section 3.2.

  • Development Plan has the meaning set forth in Section 3.2.

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

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

  • Participating Clinical Laboratory means a Clinical Laboratory which has a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan to provide services to you at the time services are rendered.

  • Implementation Plan means the schedule included in the Statement of Work setting forth the sequence of events for the performance of Services under the Statement of Work, including the Milestones and Milestone Dates.

  • 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.

  • Manufacturing Site means a location where a manufacturing

  • 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.

  • 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.

  • Clinical laboratory means a facility for the microbiological, serological, chemical, hematological, radiobioassay, cytological, immunohematological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of a disease or assessment of a medical condition.

  • 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.