Submitted:
14 May 2025
Posted:
15 May 2025
You are already at the latest version
Abstract
Keywords:
Introduction
Market Reporting Overview
- Field sampling / sample preparation and associated QAQC
- Laboratory sub-sampling, sample preparation and associated QAQC
- Laboratory assaying, analytical details and associated QAQC
- Identifying the laboratory and any relevant certification
- Verification steps by the CQP
Field Sampling/Sample Preparation and Associated QAQC5
Laboratory Sub-Sampling and Sample Preparation and Associated QAQC5
Laboratory Assaying and Analytical Steps and Associated QAQC5
Identify the Laboratory and Any Certification
Verification Steps by the CQP
- In-person audits of the laboratory to check effective Laboratory Information Systems (data management); laboratory organisation; cleanliness and potential for contamination; internal quality systems (QAQC), including adherence to agreed protocols; analytical equipment calibration methods; compliance with accreditation; and health and safety.
- Review of laboratory assay certificates and validation against the database.
- Timely analysis of QC data and subsequent liaison with the laboratory as required.
- Timely analysis of internal laboratory QC and liaison with the laboratory as required.
Conclusions
| 1 | CRIRSCO is a body whose members comprise National Reporting Organisations that are responsible for developing mineral reporting codes, standards and guidelines. Based on the established reporting codes/standards of its member countries, CRIRSCO has developed an International Reporting Template, the purpose of which is to assist with the dissemination and promotion of effective, well-tried, good practices for public reporting of Exploration Results, Mineral Resources and Ore/Mineral Reserves which is already widely adopted through national reporting codes and standards. For the purpose of this document, the term “code” will be used to describe any international reporting code or standard. |
| 2 | Exploration Results, Mineral Resources and Ore/Mineral Reserves do not “comply” with a given code; they are reported by a relevant listed entity in accordance with that code. |
| 3 | Both The JORC Code and NI 43-101/CIM are currently at various stages of revision. Whilst changes are expected, the overall matters pertinent to the reporting of assay/analytical methods are not expected to change materially. The updated JORC Code is referred to here as The JORC Code 2025. NI 43-101/CIM is at an early stage of revision. |
| 4 | For this discourse, the emphasis is on The JORC Code and NI 43-101/CIM; however, they do not differ materially from other codes in terms of reporting on the assay method used. |
| 5 | For this discourse, it is not intended to provide an extensive discussion on QAQC programmes. |
| 6 | CRMs are usually submitted pre-laboratory with a sample number so that the CRM cannot be identified. In the case of PhotonAssayᵀᴹ, CRMs are generally pre-jarred and retained at the laboratory with an instruction from the client to insert a given CRM into the stream at a given point. CRMs should be replaced and/or a different CRM used during a set period as agreed with the laboratory. CRM submission/insertion procedure will be set up and documented by the CQP. CRMs may be in the pulverised or crushed form. |
| 7 | Leading practice is to submit Check assays to a second laboratory for analysis by the same method; PhotonAssay™ in this case. Some CQPs may opt to assay via an alternative method, which is their choice. Where the Original versus Check assays disagree, then the CQP may opt to use a third or Umpire laboratory. |
References
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