Development of Test Procedure Sample Clauses

Development of Test Procedure. This procedure shall include, but not be limited to, the following subjects: arrangement and form of the test, log sheets, duration, readings to be taken, instrumentation, and method of data recording. Development of the test procedure shall generally follow the guidelines contained in ASME PTC 46, "Overall Plant Performance". [The annual Capability Test is to be conducted at an ambient temperature within 10 degrees Fahrenheit of rating dry bulb temperature. Retests shall be conducted at ambient conditions as close to rating conditions as practicable. [The previous comment is stricken, as it does not apply to the Contractor.]] The following general guidelines shall be included in the development of the test procedure for the Dedicated Unit:
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Development of Test Procedure. This procedure shall include, but not be limited to, the following subjects: arrangement and form of the test, log sheets, duration, readings to be taken, instrumentation, and method of data recording. Development of the test procedure shall generally follow the guidelines contained in ASME PTC 46, "Overall Plant Performance". The annual Capability Test is to be conducted at an ambient temperature within 10 degrees Fahrenheit of rating dry-bulb temperature. Retests shall be conducted at ambient conditions as close to rating conditions as practicable. The following general guidelines shall be included in the development of the test procedure for the Dedicated Unit:

Related to Development of Test Procedure

  • Development Program A. Development Activities to be Undertaken (Please break activities into subunits with the date of completion of major milestones)

  • Development Activities NovaDel shall not be required to commence any Development Activities until Licensee has paid at least twenty-five percent (25%) of the non-refundable License Fee described in Section 4.4.

  • Development Plan As defined in Section 3.2(a).

  • Research Plan The Parties recognize that the Research Plan describes the collaborative research and development activities they will undertake and that interim research goals set forth in the Research Plan are good faith guidelines. Should events occur that require modification of these goals, then by mutual agreement the Parties can modify them through an amendment, according to Paragraph 13.6.

  • Commercialization Reports After the First Commercial Sale of a Licensed Product anywhere in the Territory, LICENSEE shall submit to Cornell semi-annual reports on or before each February 28 and August 31 of each year. Each report shall cover LICENSEE’s (and each Affiliate’s and Sublicensee’s) most recently completed calendar half-year and shall show:

  • Research Program The term “Research Program” shall mean the research program to be undertaken by TSRI under the direction and control of the Principal Investigator as expressly set forth on Exhibit A hereto.

  • Development of the Project The Board of Managers shall take such actions as shall be required to cause either the Company or the Management Company (as defined in Section 9(b) below) to perform and complete the construction and other development work as contemplated and/or required under the NVR Purchase and Sale Agreements, or any other construction company selected by the Board of Managers (the “Development Work”), substantially in accordance with the Project Plan, at a cost to the Company not exceeding the total cost set forth in the Budget, in a manner consistent with this Agreement and all applicable laws, ordinances, rules, regulations or requirements (including, without limitation, those with respect to discrimination) of governmental authorities, and in compliance with any covenants, conditions or restrictions affecting all or any portion of the Property.

  • Project Plan Based on the Project Specifications, Omnicare CR has provided a description of services to be performed for Sponsor’s “A multi-center, randomized, double-blind, double-dummy, vehicle-controlled sequential cohort study to determine the safety of PEP005 0.025% and 0.05% topical gel in patients with actinic keratoses” (hereinafter “the Project”) and associated costs. Changes made in the Project scope, at any time during the Project, will result in a corresponding adjustment to the Project costs.

  • Development Diligence Pfizer will use its Commercially Reasonable Efforts to Develop and seek Regulatory Approval for [ * ] Product [ * ] in the Field [ * ]. Pfizer will [ * ] with respect to the Development or Regulatory Approval of Products under this Agreement.

  • Development Work Do, or cause to be done, such development and other work as may be reasonably necessary to protect from diminution and production capacity of the Mortgaged Property and each producing well thereon.

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