| Laboratory accreditation | Check whether the laboratory is accredited to ISO/IEC 17025 and whether the accreditation scope covers the requested test method and relevant sample type. | A current accreditation certificate and its detailed scope, verified with the relevant accreditation body. | The specific fire assay method and analytical determination are within scope; accreditation alone is not treated as proof that every service is accredited. |
| Method suitability | Confirm that the proposed fire assay procedure is suitable for the target element, expected concentration range, and sample matrix. | Method reference or method description, sample-mass details, and any stated limitations or interferences. | The laboratory explains the method and its limitations clearly and discusses alternatives when the sample or reporting range requires them. |
| Quality control | Ask how the laboratory monitors accuracy and precision during routine batches. | A sample batch quality-control policy describing the use of certified reference materials, blanks, and replicate or duplicate samples where appropriate. | Quality-control results are reviewed against defined acceptance criteria, and affected results are investigated when criteria are not met. |
| Technical competence | Determine whether staff are trained and authorized for the relevant preparation, assay, and measurement steps. | A description of staff qualification, training, competency assessment, and method authorization procedures. | Competence is assessed and documented for assigned tasks, with procedures available for review. |
| Proficiency testing | Ask whether the laboratory participates in relevant proficiency-testing or interlaboratory comparison programs when available. | Recent relevant participation records and a summary of how unsatisfactory results are investigated and addressed. | Results are reviewed as part of ongoing performance monitoring; participation is relevant to the method and analyte where a suitable program exists. |
| Sample preparation and handling | Review procedures for sample receipt, identification, preparation, storage, and prevention of mix-ups or contamination. | Sample-handling instructions, preparation workflow, and the laboratory's process for recording sample condition and tracking samples. | Samples are traceable through the workflow, and preparation requirements or unsuitable sample conditions are communicated before analysis. |
| Reporting and data integrity | Check whether reports identify the method, units, results, and any relevant qualifications or deviations. | A redacted sample report and an explanation of result review, corrections, record retention, and data security practices. | Reports are clear and traceable, and any changes or deviations are documented rather than silently replacing original results. |
| Detection and reporting limits | Confirm that the laboratory's reporting range and stated limits are appropriate for the intended decision or specification. | Written reporting limits, units, and clarification of how results below the reporting limit are presented. | Limits are stated for the applicable method and sample basis, and are not confused with guaranteed measurement uncertainty or a universal threshold. |