Pre-Manufacturing Phase definition

Pre-Manufacturing Phase means the phase during which the BUYER and the SUPPLIER shall prepare for the commercial manufacturing of the Products as further specified in the Agreement or Purchase Order. Tel.: +▇ ▇▇▇-▇▇▇-▇▇▇▇ ▇▇▇.▇▇▇▇▇▇.▇▇▇ 21 “Product” means each of the Product and Service Parts described in Appendix 3 and to be manufactured by SUPPLIER based on the mutually agreed upon Requirements and Specifications
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Examples of Pre-Manufacturing Phase in a sentence

  • During the Pre-Manufacturing Phase, NASI shall provide sufficient "shell" building space to house RADIOMED's activities in an efficient manner, in accordance with the projections of required space set forth in RADIOMED's business plan.

  • RADIOMED shall bear the responsibility and cost of setting up the manufacturing operation (the "Pre-Manufacturing Phase").

  • Upon completion of the Pre-Manufacturing Phase, NASI agrees to take responsibility for the ion implantation facility and to manufacture Products to mutually agreed upon Product Specifications and in accordance with forecasts provided by RADIOMED pursuant to Section 4.6 hereof.

Related to Pre-Manufacturing Phase

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

  • 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 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.

  • Manufacturing Process means any process for—

  • Manufacturing Site means a location where a manufacturing