ISO/IEC 17025 is the Laboratory Management System that specifies the general requirements for the competence to carry out tests and/ or calibrations, including sampling. It allows laboratories to implement an effective quality system and demonstrate that they are technically proficient and able to produce valid and consistent results. Laboratory customers, regulatory authorities and accreditation bodies may also use ISO/IEC 17025: 2017 in confirming or recognizing the competence.

How it benefits?

✔ Better corporate image for the laboratory
✔ Strong quality control of laboratory operations
✔ Fewer re-analyses of samples
✔ Reduction in operating costs
✔ Clear definition of roles, responsibilities, and authority
✔ Validation of traceability
✔ Provide excellent third-party recognition to your customers
✔ Competitive advantage toward your competitors
✔ Reduced customer complaint
✔ Audit and assessment activity by laboratory customers can be reduced   through third party recognition
✔ Potential increase in business due to enhanced customer satisfaction
✔ Meeting applicable compliance obligations
✔ Transition of previous management system to ISO/ IEC 17025: 2017

 

How we can collaborate?

✔ Coordinate with accreditation body
✔ Gap Analysis
✔ Documentation based on ISO /IEC 17025:2017
✔ System design and implementation
✔ Process feasibility study and report to management
✔ Internal Audit
✔ Management Review