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QA/QC

iATL prides itself on our Quality Assurance Program. We maintain all the elements of the ISO/IEC 17025 guidelines as required by NVLAP, AIHA, NYSDOH, and many other accrediting bodies. This work takes effort from every staff member and is the primary focus of designated QA personnel.

iATL’s key to success is timeliness of the quality control process and the follow-up of any corrective action to non-conformities. If QA re-analysis is not done daily, then catching mistakes and errors that are bound to occur may affect a client’s project. At iATL we are always in a 24-48 hour loop of sample analysis, QA data review, and any QC resolutions before completely validating data in order to ensure the most accurate results. This requires a team of non-analyst QA review staff.

Through our proficient quality assurance program, iATL has the means of quickly amending reports if an error is found. Analysts routinely note subtleties in their findings and communicate frequently with clients. The client never sees all of this behind the scenes attention to detail that goes into the QA process, but thoroughness is essential if you want legally defensible laboratory data


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Table of Contents QA/QC SOP Manual
Sample Submittal
Sample Archiving
Sample Disposal
Proficiency Test Results
Field / Lab Blanks
On-site Audits

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