ISO 10012-1 PDF

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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Discussion related to the importance and timing of equipment calibration.

It defines requirements relevant to the measurement management system in language that may illustrate interrelations to other parts of an overall quality management system. The competence referred to in the title of the standard relates to the competence of the 1001-21 system — not just training of personnel.

Metrology ProgramQuality Progress.

Difference Between ISO/IEC and ISO –

However if you are performing calibrations for other companies, and you are not accredited yet, I strongly recommend Z ISO focuses on the requirements of the measurement management system. 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.


Managing the Measurement SystemQuality Progress. You can consider it a system within the quality management system.

From the scope uso ISO If you want to generate true confidence of measurement that your customers and AB appreciate, then of all of those standards, I recommend Z Sorry, your blog cannot share posts by email. Skip to content Q: Managing the Measurement SystemQuality Progress Discussion related to the importance and timing of equipment calibration.

Difference Between ISO/IEC 17025 and ISO 10012

In summary, ISO is a guidance document that addresses one element namely management of a measurement system of a quality management system. Even if the organization chooses to adhere to the requirements of ISOthe certification to ISO does not imply certification to the requirements 10102-1 ISO It addresses such factors as contracts with customers, purchasing, internal auditing, and management review of the entire quality management system — ISO does not.

Denise Robitaille Vice Chair, U. ISO is a guidance document and not intended for certification.

General requirements for the competence of testing and calibration laboratoriesand I would like guidance on usage and application of these standards. It also depends on the focus of your business.

ISO defines requirements for entire quality management system that can be accredited.


ISO – Wikipedia

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.

Pricey, however that is the direction calibrations are going in the future. Correctly applied measurement, wherever and however it occurs, is an essential element of a successful business QMS. Root Cause Analysis Samples.

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. An organization, for example, could have a quality management systems that is certified to ISO ISO describes the requirements for a quality iao system that can be accredited a process comparable but different from certification.

It encompasses all aspects of the 10102-1.

I am updating the instrumentation section of a product fabrication specification to replace a cancelled military specification MIL-STD that specified calibration systems requirements.

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