Calibration laboratory definition

Calibration laboratory means an International Organization for Standardization (ISO) 17025 accredited testing laboratory that is approved by the Commissioner of Public Safety.
Calibration laboratory means an International Organization for
Calibration laboratory. ’ means a body that performs a set of operations that establish, under specified conditions, the relationship between values of quantities 20 indicated by a measuring instrument or measuring system, or values represented by

Examples of Calibration laboratory in a sentence

  • The National Physical Laboratory (NPL), or a Calibration laboratory that has been accredited by the United Kingdom Accreditation Service (UKAS), or a similarly accredited international body.

  • Calibration laboratory services for test and operational equipment will be provided by the Government on-site.

  • The Fox Calibration laboratory uses NIST traceable flow standards to ensure the highest level of accuracy and the fastest turn-around time.

  • QED The third Lemma establishes that in equilibrium there is 0 probability of a tie at a positive score.

  • Use of ‘NABL Accredited CAB Combined ILAC MRA Mark’ is voluntary and shall only be used by accredited Testing laboratory, Medical testing laboratory, Calibration laboratory and Proficiency Testing Provider (PTP) on its test report/certificate, calibration certificate/report and PT report only.

  • In intense dis- cussion with the supplier further improvements are under development and further related modi- fications are envisaged to be performed in 2008/09.The tail gas analyzer which has been used already before installation of the secondary catalyst is a multi-gas analyzer from Rosemount Analytics (Type NGA 2000, MTL3), the annual calibra- tion is done by the Czech company Calibration laboratory of emissions TESO.

  • Calibration laboratory in the field of oxygen (non exhaustive): - CSIRO (Australia).

  • NOAA, because it has the most extensive global network, and since 1996 has also operated the WMO CO2 Central Calibration laboratory, is selected as the reference.

  • An EU-funded project managed by the European Agency for Reconstruction • Calibration laboratory must have sufficient resources to act as an accredited laboratory.

  • Must be in compliance with the requirements of ANSI/NCSLI z540-1-1994 and ANSI/NCSLI z540.3 specific requirements: Calibration laboratory accreditation program.


More Definitions of Calibration laboratory

Calibration laboratory means a body that a set of operations that establish, under specified conditions, the relationship between values of quantities indicated by a measuring instrument or measuring system,or values representedby 25a material measure or reference material, and corresponding values realised bystandards whatever their uncertainty;
Calibration laboratory means a body that performs a set of operations that establish, under specified conditions, the relationship between values of quantities indicated by a measuring instrument or measuring system, or values represented by a material measure or reference material, and corresponding values realised by standards whatever their uncertainty;
Calibration laboratory means a body that performs a set of operations that
Calibration laboratory means a laboratory carrying out calibration of measuring instruments.
Calibration laboratory means a body that performs a set of operations that establishes, under specified conditions, the relationship between values of quantities indicated by

Related to Calibration laboratory

  • Calibration means the determination of (1) the response or reading of an instrument relative to a series of known radiation values over the range of the instrument, or (2) the strength of a source of radiation relative to a standard.

  • 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.

  • 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.

  • Recalibration means the adjustment of all DRG weights to reflect changes in relative resource consumption.

  • Calibration gas means a gas mixture used to calibrate gas analysers.

  • Laboratory or “LANL” means the geographical location of Los Alamos National Laboratory, a federally funded research and development center owned by the DOE / NNSA.

  • cGMP means current Good Manufacturing Practices as specified in the United States Code of Federal Regulations, ICH Guideline Q7A, or equivalent laws, rules, or regulations of an applicable Regulatory Authority at the time of manufacture.

  • 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.

  • 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.

  • Clinical nurse specialist means a registered nurse with relevant post-basic qualifications and 12 months’ experience working in the clinical area of his/her specified post-basic qualification, or a minimum of four years’ post-basic registration experience, including three years’ experience in the relevant specialist field and who satisfies the local criteria.

  • Dental laboratory means a person, firm or corporation

  • Testing means that element of inspection that determines the properties or elements, including functional operation of materials, equipment, or their components, by the application of established scientific principles and procedures.

  • Technical Specifications A specification in a document defining the characteristics of a product or a service, such as the quality levels, the environmental and climate performance levels, the design for all needs, including accessibility for people with disabilities, and the evaluation of conformity, of product performance, of the use of the product, safety or dimensions, as well as requirements applicable to the product as regards the name by which it is sold, terminology, symbols, testing and test methods, packaging, marking or labelling, instructions for use, the production processes and methods at every stage in the life cycle of the supply or service, as well as the evaluation and conformity procedures;

  • Quality system means documented organizational procedures and policies: internal audits of those policies and procedures: management review and recommendation for quality improvement.”

  • 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.

  • Finished water means the water that is introduced into the distribution system of a public water system and is intended for distribution and consumption without further treatment, except as treatment necessary to maintain water quality in the distribution system (e.g., booster disinfection, addition of corrosion control chemicals).

  • technical specification means a document that prescribes technical requirements to be fulfilled by a product, process or service;

  • Assay means a laboratory analysis of Crude Petroleum to include the following: A.P.I. Gravity, Reid vapor pressure, composition, pour point, water and sediment content, sulfur content, viscosity, distillation, hydrogen sulfide, flash/boiling point and other characteristics as may be required by Carrier.

  • GMP means the amount proposed by Contractor and accepted by Owner as the maximum cost to Owner for construction of the Project in accordance with this Agreement. The GMP includes Contractor’s Construction Phase Fee, the General Conditions Cost, the Cost of the Work, and Contractor’s Contingency amount.

  • 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.

  • health and safety specification means a site, activity or project specific document prepared by the client pertaining to all health and safety requirements related to construction work;

  • 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.

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

  • Drug Substance means an active ingredient that is intended to furnish pharmacological activity or other direct effect in the diagnosis, cure, mitigation, treatment, or prevention of disease or to affect the structure or any function of the human body, but does not include intermediates used in the synthesis of such ingredient.

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