Testing and Calibration Laboratories
ISO 17025
Every testing and calibration laboratory necessarily wants reliable results, which makes them highly trustworthy in front of the key stakeholders. In this aspect, ISO 17025 enables organizations to showcase that they operate efficiently and generate valid results which can escalate the confidence in their work among local and international end consumers.
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ISO 17025 - Testing and Calibration Laboratories
Every testing and calibration laboratory necessarily wants reliable results, which makes them highly trustworthy in front of the key stakeholders. In this aspect, ISO 17025 enables organizations to showcase that they operate efficiently and generate valid results which can escalate the confidence in their work among local and international end consumers.
Furthermore, it also bridges the cooperation between laboratories and other bodies by generating wider acceptance of results across the countries and removing the hassle of retesting again and again.
Key points regarding ISO 17025
ISO 17025 is published by the international organization for standardization (ISO), in 1999, to promote or enable laboratories to demonstrate valid testing results. The standard definition of ISO 17025 is as follows:
“ISO 17025 is a standard for laboratory competence which highly covers the calibration and testing performed by using laboratory-developed standard or non-standard methods.”
ISO 17025 is applicable to all laboratories regardless of the size or scope of testing and calibration practices.
Structure of ISO 17025
The 2017 version of ISO/IEC 17025 has modified this structure to be Scope, Normative References, Terms and Definitions, General Requirements, Structural Requirements, Resource Requirements, Process Requirements, and Management System Requirements.
- General Requirements and Structural Requirements are pertinent to the organization of the laboratory itself.
- Resource Requirements entail issues related to the people, plant, and other organizations used by the laboratory to produce technically valid results.
- Process Requirements are the heart of this version of the standard as they describe the activities to ensure that results are based on accepted science and aimed at technical validity.
- Management System Requirements are those steps taken by the organization to give itself QMS tools to support the work of its people in the production of technically valid results.
The deployment of ISO 17025 is followed by the Plan-Do-Check-Act Methodology.
Benefits of ISO 17025
The core benefits of practicing the essence of ISO 17025 standard are given below:
Global reputation of ISO 17025 compliant organziation
Surpassing the stakeholders requirements and expectations
Highly Efficient testing and calibration expertise
Potential increased economic growth
Improved Lab Testing Environment
Cost Reduction
Help meeting regulatory requirements and compliance of other standards
More efficient documentation of techniques, methods, and procedures
Steps to World Class ISO 17025 Consultancy
Step 1
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Step 2
Our ISO Consultants will review your query and send detailed proposal in the light of query.
Step 3
Formal project will roll out once the proposal is accepted.
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Our premium consultancy framework caters to the turnkey requirement of complete ISO 17025 effective implementation, in the organization, followed by the necessary ongoing monthly support for evaluation and concerning documentation. In this regard, we provide solutions and make strategies through data-driven analytics for maximizing performances and production capabilities, which can complement organizational long-term strategic quality goals.
Likewise, the end-to-end support for ongoing training and mentoring to the organizational personnel is one of the many unique benefits of our consultancy intervention model.
Conclusion
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