Approved testing laboratory definition

Approved testing laboratory means a testing laboratory that meets criteria for electrical product evaluation established by the Director of the Department of Consumer and Business Services with the approval of the Electrical and Elevator Board under ORS 479.730.
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Approved testing laboratory means a testing laboratory that meets criteria for electrical
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Approved testing laboratory means a laboratory approved for the purposes of regulation 6(1) (e)(i) by a competent authority;
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Examples of Approved testing laboratory in a sentence

  • Certifications of Calibration: Approved testing laboratory certificate if pressure gauge for hydrostatic test has been previously used.

  • Certification of Calibration: Approved testing laboratory certificate if pressure gauge for hydrostatic test has been previously used.

  • Our results could also potentially be adapted to provide subgrid ISM/star formation prescriptions for use in cosmological simulations of galaxy formation, but this too should be approached with care since the ratio of diffuse to gravitationally-bound gas is computed not for a local three-dimensional zone but forza vertically-integrated disk.

  • Validation by a NIST Approved testing laboratory provides assurance that implementation errors do not exist.

  • Testing Agency: Approved testing laboratory selected and paid by Owner.

  • Approved testing laboratory shall be Soil Testing Service (916)649-9331, P.O. Box 340296, Sacramento, CA 95834, or approved equal.

  • Approved testing laboratory means a laboratory approved by the Commission pursuant to subsection 9B-72.100(3), F.A.C., to test products for compliance with the standards specified in the Code.

  • Floor Stone Testing Results: Submit test reports from qualified independent, Los Angeles City Approved testing laboratory indicating and interpreting test results relative to compliance of stone flooring with requirements specified for slip resistance.

  • Test Reports: Submit test reports from qualified independent, L.A. City Approved testing laboratory indicating and interpreting test results relative to compliance of tile products with requirements specified for slip resistance.

  • Final approval shall be evidenced by a certificate of approval issued by an Approved testing laboratory certifying full compliance with the AWWA standards and FCCC and HR specifications.


More Definitions of Approved testing laboratory

Approved testing laboratory means a laboratory which meets Federal requirements and is certified to administer such testing.
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Approved testing laboratory means the FCCCHR of the University of Southern California; or the director approves another independent laboratory having equivalent facilities for both laboratory and field evaluation of backflow prevention assemblies.
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Approved testing laboratory means a person or entity that is competent and possesses the necessary facilities, as determined by the Department, to investigate and evaluate backflow prevention assemblies.
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Related to Approved testing laboratory

  • Testing laboratory means a laboratory, facility, or entity in the state that offers or performs tests of cannabis or cannabis products and that is both of the following:

  • 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.

  • Independent testing laboratory means an independent organization, accepted by the Contracting Officer, engaged to perform specific inspections or tests of the work, either at the site or elsewhere, and report the results of these inspections or tests.

  • 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.

  • 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.

  • Dental laboratory means a person, firm or corporation

  • Non-Participating Clinical Laboratory means a Clinical Laboratory which does not have a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan provide services to you at the time services are rendered.

  • Certified laboratory means a laboratory that is on an approved list issued by us.

  • Approved clinical trial means a phase I, phase II, phase III, or phase IV clinical trial that is conducted in relation to the prevention, detection, or treatment of cancer or other life-threatening disease or Condition and is described in any of the following:

  • Clinical review criteria means the written screening procedures, decision abstracts, clinical protocols, and practice guidelines used by a health carrier to determine the necessity and appropriateness of health care services.

  • Drug test means a test designed to detect the illegal use of a controlled substance.

  • Genetic testing means an analysis of genetic markers to exclude or identify a man as the father or a woman as the mother of a child. The term includes an analysis of one or a combination of the following:

  • Root Cause Analysis is the formal process, specified in the Policy and Procedures Manual, to be used by Supplier to diagnose problems at the lowest reasonable level so that corrective action can be taken that will eliminate, to the extent reasonably possible, repeat failures.

  • Phase I Clinical Study means a human clinical study of a product, the principal purpose of which is a preliminary determination of safety in healthy individuals or patients, as described in 21 C.F.R. 312.21(a).

  • Phase 2 Clinical Trial means a human clinical trial of a product in any country that would satisfy the requirements of 21 C.F.R. 312.21(b) and is intended to explore a variety of doses, dose response, and duration of effect, and to generate initial evidence of clinical safety and activity in a target patient population, or a similar clinical study prescribed by the relevant Regulatory Authorities in a country other than the United States.

  • Participating Certified Clinical Nurse Specialist means a Certified Clinical Nurse Specialist who 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.

  • Non-Participating Certified Clinical Nurse Specialist means a Certified Clinical Nurse Specialist who does not have 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.

  • Cannabis testing facility means an entity registered by

  • Phase I Clinical Trial means a clinical trial conducted in healthy humans or patients, which clinical trial is designed to establish the safety, drug-drug interactions and/or pharmacokinetics of an investigational drug given its intended use, and to support continued testing of such drug in Phase II Clinical Trials.

  • Penetration Testing means security testing in which assessors mimic real-world attacks to identify methods for circumventing the security features of an application, system, or network. (NIST SP 800-115)

  • Drug use test means a scientifically substantiated method to test for the presence of illegal or performance-enhancing drugs or the metabolites thereof in a person’s urine.

  • Phase 1 Clinical Trial means a Clinical Trial of a Product on sufficient numbers of normal volunteers and/or patients that is designed to establish that such Product is safe for its intended use and to support its continued testing in Phase 2 Clinical Trials. For purposes of this Agreement, ‘initiation’ of a Phase 1 Clinical Trial for a Product means the first dosing of such Product in a human subject in a Phase 1 Clinical Trial.

  • Phase I Trial means a clinical trial of a Licensed Product in human patients conducted primarily for the purpose of determining the safety, tolerability and preliminary activity of the Licensed Product, including, without limitation, for determining the maximum tolerated dose, or optimal dose. For purposes of this Agreement, a Phase I trial shall specifically exclude a study in healthy volunteers.

  • Cardiopulmonary resuscitation or "CPR" means artificial ventilation or external

  • Phase II Clinical Study means a human clinical study of a product initiated to determine the safety and efficacy in the target patient population, as described 21 C.F.R. 312.21(b).

  • Corrective Measure The contractor shall repair and deficiencies which do not meet the performance guideline.