ISO Quality Assurance Requirements for Measuring Equipment – Part 1 : Metrological Confirmation System for Measuring Equipment. ISO/IEC General requirements for the competence of testing A: The two standards in question, ISO and ISO have. ISO INTERNATIONAL. STANDARD. ISO. First edition .. and replaces ISO and ISO , of which it.
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ISO focuses on the requirements of the measurement management system.
However if you are performing calibrations for other companies, and you are 100121 accredited yet, I strongly recommend Z Root Cause Analysis Samples. Sorry, your blog cannot share posts by email. It also depends on the focus of your business.
Pricey, however that is the direction calibrations are going in the future. An organization, for example, could have a quality management systems that is certified to ISO Correctly applied measurement, wherever and however it occurs, is an essential element of a successful business QMS.
Denise Robitaille Vice Chair, U. Even if the organization chooses to adhere to the requirements of ISOthe certification to ISO does not imply certification to the 10012-1 of ISO Managing the Measurement SystemQuality Progress. General requirements for the competence of testing and calibration laboratoriesand I would like guidance on usage and application of these standards.
Difference Between ISO/IEC 17025 and ISO 10012
Metrology ProgramQuality Progress. Discussion related to the importance and timing of equipment calibration. While the scope of both documents includes language that can perhaps cause confusion, what follows is the salient text from both that illuminates the difference between the two.
The competence referred to in the title of the standard relates to the competence of the entire system — not just 10012- of personnel. It defines requirements relevant to the measurement management system in language that may illustrate interrelations to other parts of an overall quality management system.
ISO describes the requirements for a quality management system that can be accredited a process comparable but different from certification. ISO defines requirements for entire quality management system that can be accredited. If you want to generate true confidence of measurement that your customers and AB appreciate, then of all of those standards, I recommend Z It encompasses all aspects of the laboratory.
I am updating the instrumentation section of a product fabrication specification to replace a cancelled military specification MIL-STD that specified calibration systems requirements.
Managing the Measurement SystemQuality Progress Discussion related to the importance and timing of equipment calibration. In summary, ISO is a guidance document that addresses one element namely management of a measurement system of a quality management system.
ISO is a guidance document and not intended for certification. If calibrations are just a subsidiary aspect of your business, then spending the money to get accredited may not be necessary, especially if its for internal use only.
Difference Between ISO/IEC and ISO –
It addresses such factors as contracts with customers, purchasing, internal auditing, and management review of the entire quality management system — ISO does not. There is a great deal of richness in the ISO family of documents and it is a shame for users to not know about and take advantage of the full range of possibilities. From the scope of ISO You can consider it a system within the quality management system.
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