We design and implement Quality Management Systems to meet the requirements of ISO/IEC 17025 Accreditation

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How may we assist you with preparing your Laboratory for ISO Accreditation?

We can provide full-service implementation through your accreditation audit, or provide assistance with completing one of more of the following requirements:

• √ Preparation of a Quality Management System Plan and Manual

• √ Preparation of Documented Controls for Documents, Internal Auditing, Non-conformity, Corrective Actions and Records

• √ Preparation of Documented Guidance for Process Measurements, Quality Objectives, Reporting, Risk Assessments, Security and Safety.

• √ ISO 17025 Gap Assessment Audit and Report (excellent for initial planning or for pre-audit assessment)

• √ Internal Audit of your ISO 17025 Laboratory Quality Management System

• √ Quality Management Software Tools (QMSCAPA) for …

  √ Corrective Actions,

  √ Measuring Quality Objectives,

  √ Recording Competency and Training,

  √ Recording Non-conformance,

  √ Tracking Customer Feed-back

  √ Tracking Monitoring & Measuring Devices for Calibration and Maintenance

ISO/IEC 17025 specifies the general requirements for the competence to carry out tests and/or calibrations, including sampling. It covers testing and calibration performed using standard methods, non-standard methods, and laboratory-developed methods.

• The standards full title is “General Requirements for the Competence of Testing and Calibration Laboratories”;
• If a testing and calibration laboratory complies with ISO 17025, it will also operate in accordance with ISO 9001. However, certification against ISO9001 does not itself demonstrate the competence of the laboratory to produce technically valid data and results;
• There is a discussion document ISO/IEC DIS 17025 to offer guidance on implementation;
• The standard can also covers in-house laboratories or testing operations where assurance of results is at a premium;
• It applies to organizations that want to assure their customers of precision, accuracy and repeatable results;
• It may be important to first-, second- and third-party laboratories, and laboratories where testing and/or calibration forms part of inspection and product certification;
• ISO/IEC 17025:2005 is applicable to all laboratories regardless of the number of personnel or the extent of the scope of testing and/or calibration activities;
• When a laboratory does not undertake one or more of the activities covered by ISO/IEC 17025:2005, such as sampling and the design/development of new methods, the requirements of those clauses do not apply;
• Laboratory customers, regulatory authorities and accreditation bodies may also use it in confirming or recognizing the competence of laboratories;
• ISO/IEC 17025 was formerly ISO Guide 25 & EN45001;
• Compliance with regulatory and safety requirements on the operation of laboratories is not covered by ISO/IEC 17025:2005;
• ISO/TS 16949, the Automotive Quality Management System has stipulated that first tier suppliers of calibration and test services be ISO 17025 certified, and that suppliers upstream of them be compliant.
• State of California, Bureau of Medical Marijuana Regulation in the Department of Consumer Affairs