Quality-system review
Review the quality manual, document control, internal audits, management review, complaints, and corrective action.
ILC helps laboratories connect state rules, ISO 17025 systems, methods, training, equipment, samples, data, deviations, and quality records.
Clear sample custody and traceability
Controlled methods and quality records
Training tied to authorized work
A practical path through findings and corrective actions
The exact engagement depends on your license, locations, stage, and internal capacity.
Review the quality manual, document control, internal audits, management review, complaints, and corrective action.
Follow receipt, accessioning, storage, preparation, analysis, result review, reporting, retention, and disposal.
Check training, competency, authorization, calibration, maintenance, standards, and environmental records.
Practice pulling a sample file and explaining the chain of work from custody through reported result.
Most problems show up when what staff do, what the system records, and what the written procedure says no longer match.
Training exists, but the record does not show who approved an analyst for a method.
Custody, preparation, instrument, and reporting records cannot be followed as one file.
The immediate error is addressed without testing why the system allowed it.