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STQC provides calibration services, such as Electro Technical Calibration, Non-Electrical Calibration, High Precision Calibration, Onsite Calibration and Medical Equipment Calibration. Multiple STQC laboratories have obtained national and international accreditations and recognitions in the testing and calibration sector.
National Accreditation Board for Testing and Calibration Laboratories (NABL) provides accreditation to Conformity Assessment Bodies (Laboratories) in India.NABL Schemes include Accreditation (Recognition) of Technical competence of testing, calibration, medical testing laboratories, Proficiency testing providers (PTP) & Reference Material Producers (RMP) for a specific scope following ISO/IEC ...
ISO/IEC 17025 General requirements for the competence of testing and calibration laboratories is the main standard used by testing and calibration laboratories. In most countries, ISO/IEC 17025 is the standard for which most labs must hold accreditation in order to be deemed technically competent.
The formal definition of calibration by the International Bureau of Weights and Measures (BIPM) is the following: "Operation that, under specified conditions, in a first step, establishes a relation between the quantity values with measurement uncertainties provided by measurement standards and corresponding indications with associated measurement uncertainties (of the calibrated instrument or ...
A common label for certifying that a device has been tested. In electrical safety testing, portable appliance testing (PAT, PAT inspection or PAT testing) is a process by which electrical appliances are routinely checked for safety, commonly used in the United Kingdom, Ireland, New Zealand and Australia.
Secondary reference standards: Reference standards calibrated against and traceable to primary WHO materials and intended for use in routine tests; Reference reagent: a WHO reference standard, the activity of which is defined by WHO in terms of a unit; For chemical substances some pharmacopoeias [10] use the WHO terms [11]
The physical appearance of the DMR can be a binder with documents, a document that can refer to other documents, or the same concepts in a computer as documents in a database. Labels, Instructions for Use, drawings, Certificates of Conformity, and other documents might form part of a DMR.
Verification is intended to check that a product, service, or system meets a set of design specifications. [6] [7] In the development phase, verification procedures involve performing special tests to model or simulate a portion, or the entirety, of a product, service, or system, then performing a review or analysis of the modeling results.