Conformity evaluation definition

Conformity evaluation means the entire process from the applicability analysis through the conformity determination that is used to demonstrate that the federal action conforms to the requirements of this regulation.
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Conformity evaluation means a procedure through which is to be given a written guarantee showing that one product, process or service is in accordance with specified requests.
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Examples of Conformity evaluation in a sentence

  • The emission reduction credits do not have to be quantified before the reduction strategy is implemented, but must be quantified before the credits are used in the General Conformity evaluation.

  • The first step in a General Conformity evaluation is an analysis of whether the requirements apply to a proposed federal action in a nonattainment or a maintenance area.

  • The General Conformity regulations establish certain procedural requirements that must be followed when preparing a General Conformity evaluation.

  • The procedures required for the General Conformity evaluation are similar but not identical to those for conducting an air quality impact analysis pursuant to NEPA regulations.

  • The EIR/EIS was prepared to comply with both NEPA and CEQA.The General Conformity regulations establish certain procedural requirements that must be followed when preparing a General Conformity evaluation and are similar but not identical to those for conducting an air quality impact analysis under NEPA regulations.

  • Conformity evaluation for federal installations with facility-wide emission budgets.

  • The EPA is clarifying in 40 CFR 93.150 the General Conformity evaluation for treatment of emissions from actions with emissions originating in more than one nonattainment or maintenance area.

  • Conformity evaluation according to Appendix VIII.Marking CE Ex II2GDc.-EN 15714-3 Pneumatic Part-Turn Actuators For Industrial Valves Applied harmonized and non-harmonized technical Standards:- EN 13463-1:2001, EN 1127-1.

  • Conformity evaluation according to Appendix VIII.Marking CE Ex II2GDc.-EN 15714-3 Applied harmonized and non-harmonized Technical Standards: - See ACTREG’s Catalogue & Assembly & Maintenance Procedures.- EN 13463-1:2001, EN 1127-1.

  • FRA conducted a General Conformity evaluation consistent with 40 C.F.R. Part 93 Subpart B.

Related to Conformity evaluation

  • Clinical evaluation means a systematic and planned process to continuously generate, collect, analyse and assess the clinical data pertaining to a device in order to verify the safety and performance, including clinical benefits, of the device when used as intended by the manufacturer;

  • Site evaluation means a comprehensive analysis of soil and site conditions for an OWTS.

  • conformity assessment means the process demonstrating whether the requirements of this Regulation relating to a device have been fulfilled;

  • Medical evaluation means the process of assessing an individual's health status that includes a medical history and a physical examination of an individual conducted by a licensed medical practitioner operating within the scope of his license.

  • Performance evaluation means evaluation of work and program participation as well as other areas of behavior.

  • Independent educational evaluation means an evaluation conducted by a qualified examiner who is not employed by the public agency responsible for the education of the child in question.

  • Financial Reporting Measure means any measure determined and presented in accordance with the accounting principles used in preparing the Company’s financial statements, and any measures derived wholly or in part from such measures, including GAAP, IFRS and non-GAAP/IFRS financial measures, as well as stock or share price and total equityholder return.

  • Root Cause Analysis Report means a report addressing a problem or non-conformance, in order to get to the ‘root cause’ of the problem, which thereby assists in correcting or eliminating the cause, and prevent the problem from recurring.

  • Summative evaluation means the comprehensive, end-of-cycle appraisal and shall incorporate the results of the minimum required observations, any additional observations, and required component-level data. At the discretion of the Evaluator, it may also include additional Announced, Unannounced, or Short observation data beyond the required observation data provided by other Credentialed Observers.

  • Web Site Accessibility Standards/Specifications means standards contained in Title 1 Texas Administrative Code Chapter 206.

  • Cost Analysis means the evaluation of cost data for the purpose of arriving at estimates of costs to be incurred, prices to be paid, costs to be reimbursed, or costs actually incurred.

  • Financial Reporting Measures means measures that are determined and presented in accordance with the accounting principles used in preparing the Company’s financial statements, and all other measures that are derived wholly or in part from such measures. Stock price and total shareholder return (and any measures that are derived wholly or in part from stock price or total shareholder return) shall, for purposes of this Policy, be considered Financial Reporting Measures. For the avoidance of doubt, a Financial Reporting Measure need not be presented in the Company’s financial statements or included in a filing with the SEC.

  • NERC Reliability Standards means the most recent version of those reliability standards applicable to the Generating Facility, or to the Generator Owner or the Generator Operator with respect to the Generating Facility, that are adopted by the NERC and approved by the applicable regulatory authorities, which are available at xxxx://xxx.xxxx.xxx/files/Reliability_Standards_Complete_Set.pdf, or any successor thereto.

  • Web Site Accessibility Standards/Specifications means standards contained in Title 1 Texas Administrative Code Chapter 206.

  • Technical Standards means the technical standards set out in paragraph 2.5 of the Order Form;

  • Environmental and Social Standards or “ESSs” means, collectively:

  • Approved laboratory means a laboratory that is listed in the national conference of interstate milk shipments list of sanitation compliance and enforcement ratings distributed by the United States food and drug administration and as approved by the director.

  • Goods Specification means any specification for the Goods, including any related plans and drawings, as set out in the Order or otherwise agreed in writing by Get Living and the Supplier;

  • SOP means a standard operating procedure.

  • Sales Report means a report in substantially the form set forth in Exhibit B “Royalty Report Form”.

  • Year 2000 Compliance has the meaning set forth in section 17.29 of the Management Agreement.

  • Adverse System Impact means a negative effect that compromises the safety or reliability of the electric distribution system or materially affects the quality of electric service provided by the electric distribution company (EDC) to other customers.

  • Reliability Standards means the criteria, standards, rules and requirements relating to reliability established by a Standards Authority.