In the forensic industry, if a new standard could reduce doubt in the courtroom and enhance scientific analysis, every director would want to implement it into their laboratory. ISO 17025 accreditation does just that. Gaining ISO 17025 accreditation is an internationally recognized achievement that enhances the reputation of the laboratory and testifies to the value of continuously reaching excellence. But, as all laboratory directors know, receiving accreditation is not a single milestone, but an ongoing process.

If you are planning a new facility or renovation, this process starts as early as the design phase and continues as far as impacting the daily activities of the director, quality manager, and every staff member.

The new standard for laboratory accreditation is ISO 17025. It provides a framework for the specific needs of organizations that want to control their laboratory processes. The requirements of ISO 17025 encompass all aspects of laboratory management, including calibration procedures, analytical testing proficiency, report generation and record keeping, and to ensure calibrations are performed by properly trained personnel using controlled test methods and procedures. The bottom line is that to be ISO accredited, the laboratory must not only be consistent in their procedures, but have a properly designed facility.

This article focuses on Good Laboratory Practice (GLP) that when implemented, will assist in the process of gaining accreditation. GLP is the opportunity to incorporate design specifications required for ISO before even applying for accreditation.