Managing a testing or calibration laboratory in an ISO/IEC 17025:2017 quality environment requires the creation of a wide range of documents and records.
To be effective your Quality management documents, must be kept up to date, and be sufficiently detailed and robust, to avoid room for misinterpretation and misunderstanding. In this regard we can develop protocols to validate your laboratory’s procedures.
Having your quality documents reviewed by a third party, who is distant from your laboratory’s operations, can identify gaps and ambiguities that would otherwise be missed.
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