ISO / IEC 17025 : Testing and Calibration Lboratories

ISO 17025 enables laboratories to demonstrate that they operate competently and generate valid results, thereby promoting confidence in their work both nationally and around the world.

It also helps facilitate cooperation between laboratories and other bodies by generating wider acceptance of results between countries. Test reports and certificates can be accepted of results between countries. Test reports and certificates can be accepted from one country to another country without the need for further testing, which, in turn, improves international trade.

The study of this standard explains a lot of things in the favour of laboratory operations. These are the main forces behind the entire standardization of ISO 17025 certification.

1. Scientific Method

Already approved scientific projects are approachable within the principle. It also states that experts must be present while doing such works.

2. Capacity

A laboratory must carry the concept of keeping everything online. It starts with quality control, equipment, facilities, and numerous other procedures. Competent results are available for sure.

3. Impartiality of Conduct

While conducting the operations, there may be the chance to execute a few tests. In any circumstance, you can’t override the concept of scientific approach.

4. Exercise of Responsibility

This principle allows persons to utilize their required skills at different levels of this organization.

5. Repeatability of Tests

The entire phenomenon is on the development of the same results.

6. Traceability of Measurement

This is the phase that expands the purpose within the laboratory.

The procedure for the accreditation of the ISO 17025 accredited labs list is in itself an easy one, considering that it requires only few steps or requirements to complete.

• Step 1 - Executive and Management Overview/ Planning
• Step 2 - Contact a consultant an ISO 17025 to guide you through ISO 17025 implementation. Discuss with the consultant to create a checklist for compliance. In case if one is already there, then revising the checklist.
• Step 3 - Conduct an internal audit to assess all the possible ways of conformity.
• Step 4 - A list of non-conformities is created, and they are composed to the specific clause mentioned in ISO 17025 standard.
• Step 5 - Make the required changes in the process or the documentation to eliminate non conformities.
• Step 6 - Schedule an audit by Certified ISO 17025 lead auditor.
• Step 7 - Make the required changes in the process or the documentation to eliminate non conformities.
• Step 8 - If any kind of non-conformity still arises, schedule a follow up audit.