Method validation and verification
Methods are evaluated for fitness for purpose before routine use, including relevant performance characteristics and matrix considerations.
Peak Analytical is an ISO/IEC 17025 accredited independent third-party testing laboratory, with accreditation implementation supported by IMSM.
Peak Analytical operates as an ISO/IEC 17025 accredited independent third-party testing laboratory. Our accreditation implementation and quality-management framework are supported by IMSM.
ISO/IEC 17025 is an international standard for testing and calibration laboratories. Accreditation assesses whether a laboratory operates impartially, uses technically competent personnel, controls equipment and methods, and produces valid results.
The exact controls used depend on the method and quality system. These sections explain common ISO/IEC 17025 concepts in plain language.
Methods are evaluated for fitness for purpose before routine use, including relevant performance characteristics and matrix considerations.
Where applicable, results are linked through documented calibrations, reference materials, and measurement standards.
Critical equipment is identified, maintained, calibrated or verified, and protected from use when performance is questionable.
Personnel are trained, evaluated, and authorized for the activities they perform.
Suitable blanks, controls, standards, replicates, system-suitability checks, or other controls are used as required by the method.
External comparisons or suitable alternatives help evaluate laboratory performance where available and appropriate.
Nonconforming work is controlled, investigated, corrected, and assessed for possible impact on reported results.
Current methods, procedures, forms, and records are controlled so personnel use authorized versions.
Risks to impartiality are managed, and client information is protected according to applicable obligations.
Peak Analytical should maintain documented processes for receiving, evaluating, and resolving complaints and appeals without compromising impartiality.
Include the Test ID, sample identifier, report date, and a clear description of the concern.