The document discusses considerations around quality assurance/quality control (QA/QC) and sample security in mining exploration. It outlines how QA/QC and sample security practices have strengthened since the Bre-X scandal, with regulatory bodies now requiring strict policies. However, hundreds of private exploration companies may lack sufficient QA/QC protocols. The authors argue that independent quality control, including blind insertion of control samples, is needed to objectively assess precision and accuracy, even when laboratories have internal quality control. They also discuss how blind insertion and maintaining sample security/chain of custody can be compatible goals.
The document discusses considerations around quality assurance/quality control (QA/QC) and sample security in mining exploration. It outlines how QA/QC and sample security practices have strengthened since the Bre-X scandal, with regulatory bodies now requiring strict policies. However, hundreds of private exploration companies may lack sufficient QA/QC protocols. The authors argue that independent quality control, including blind insertion of control samples, is needed to objectively assess precision and accuracy, even when laboratories have internal quality control. They also discuss how blind insertion and maintaining sample security/chain of custody can be compatible goals.
The document discusses considerations around quality assurance/quality control (QA/QC) and sample security in mining exploration. It outlines how QA/QC and sample security practices have strengthened since the Bre-X scandal, with regulatory bodies now requiring strict policies. However, hundreds of private exploration companies may lack sufficient QA/QC protocols. The authors argue that independent quality control, including blind insertion of control samples, is needed to objectively assess precision and accuracy, even when laboratories have internal quality control. They also discuss how blind insertion and maintaining sample security/chain of custody can be compatible goals.
The document discusses considerations around quality assurance/quality control (QA/QC) and sample security in mining exploration. It outlines how QA/QC and sample security practices have strengthened since the Bre-X scandal, with regulatory bodies now requiring strict policies. However, hundreds of private exploration companies may lack sufficient QA/QC protocols. The authors argue that independent quality control, including blind insertion of control samples, is needed to objectively assess precision and accuracy, even when laboratories have internal quality control. They also discuss how blind insertion and maintaining sample security/chain of custody can be compatible goals.
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Considerations on QA&QC and Sample Security
Armando Simn and Greg Gosson
AMEC Americas Limited Sampling 2008, 27-29 May 2008, Perth, Western Australia Presentation Outline Introduction QA/QC and Sample Security Sampling 2008, 27-29 May 2008, Perth, WA 2 Introduction Objective assessment of precision Why blind insertion of control samples? QC versus Sample Security Recommendations Introduccin "Bre-X Minerals geologist The Bre The Bre--X Affair X Affair Sampling 2008, 27-29 May 2008, Perth, WA 3 "Bre-X Minerals geologist Michael de Guzman, centre, conducts a survey with his colleagues at the Busang-2 field in Indonesia in this March 1997 picture. (Associated Press/Gatra Magazine) Before Bre-X - Usually lacking QAfQA programs, or with insufficient coverage, even when run by major companies - Usually loose security policies, little concern about General Trends in QAJQC and Sample Security Introduccin Sampling 2008, 27-29 May 2008, Perth, WA 4 - Usually loose security policies, little concern about possible frauds After Bre-X - Strict QAfQC policies required by regulatory bodies - Strict security policies, chain of custody, strong scrutiny - !ncreasing interest from exploration and mining companies in complying with new regulations Quality in NI 43-101 All written information of scientific or technical nature related to mining projects should: Introduccin Sampling 2008, 27-29 May 2008, Perth, WA 5 Specify if a Qualified Person verified the data on which this information is based, including sampling, assaying and tests Describe the quality assurance program and the quality control measures Describe the nature and limitations of such verification Explain any deficiencies detected during the verification Quality in JORC A Competent Person report should: Introduccin Sampling 2008, 27-29 May 2008, Perth, WA 6 Describe the nature, quality and appropriate selection of sampling and analytical procedures Describe the quality control procedures, including the insertion of standards, blanks, duplicates and external checks Assess the accuracy and precision levels attained during the project However, quality of geological data is a matter of concern not only for companies working under NI43-101, JORC or other widely recognized codes: Introduccin Sampling 2008, 27-29 May 2008, Perth, WA 7 NI43-101, JORC or other widely recognized codes: Hundreds (or thousands?) of private exploration companies, mines and laboratories are involved in exploration and mining all over the world. Consequence of Lack of QC Protocols (or Poor QC Protocols) Entire drilling campaign data may have to be partially or totally excluded from the resource estimation databases Quality Control Sampling 2008, 27-29 May 2008, Perth, WA 8 totally excluded from the resource estimation databases The estimated resources may be down-graded If QC data were not timely processed, then only a forensic analysis can be done. Quality Control Hence, we need comprehensive geological QC programs!!! Monitoring the main quality parameters, and taking Sampling 2008, 27-29 May 2008, Perth, WA 9 Monitoring the main quality parameters, and taking appropriate measurements (if necessary) Assessing precision (sampling, sub-sampling, analytical) Assessing accuracy Assessing contamination during preparation and assaying Assessment of Precision (1) ISO 3534-1 defines precision as "the closeness of agreement between independent test results obtained under stipulated Quality Control Sampling 2008, 27-29 May 2008, Perth, WA 10 between independent test results obtained under stipulated conditions. Repeatability conditions are fulfilled when re-sampling occurs in the same sampling intervals, with the same sampling procedure, when samples are processed with the same equipment and the same preparation procedure, and are assayed with the same measuring instrument, under the same measurement conditions, and are repeated over a short period of time. Assessment of Precision (2) Therefore, an objective assessment of precision on repeatability conditions requires that the original and the duplicate samples be included within the same batch. Quality Control Sampling 2008, 27-29 May 2008, Perth, WA 11 included within the same batch. However, at least for preparation and pulp duplicates this is seldom accomplished: Duplicates are usually inserted in another batch, sometimes months (or years) later, or Duplicates are submitted to another laboratory, alleguedly to assess precision. Is Independent QC Actually Needed? (1) Internationally certified and competently managed laboratories have their own internal QC protocols, and the assay certificates Quality Control Sampling 2008, 27-29 May 2008, Perth, WA 12 have their own internal QC protocols, and the assay certificates commonly include the results of at least some of the internal laboratory QC. However, most laboratories will only reveal those checks that pass their internal controls, but not the failures. Problems with sampling, preparation and assaying are seldom the result of dishonest attempts to hide or falsify certain facts, but rather unintentional errors or bias introduced by improper sample collection, preparation and assaying. Is Independent QC Actually Needed? (2) However, from time to time we witness some deceptive practices at the laboratory, like: Quality Control Sampling 2008, 27-29 May 2008, Perth, WA 13 Altering the sample order: Preparing all the ordinary samples first, and leaving the blanks to be processed at the end, after cleaning the equipment Correcting the values of the whole batch to compensate for the deviations from the CRM certified value. Is Independent QC Actually Needed? (3) Unfortunately, regardless of the good intentions of laboratory Quality Control Sampling 2008, 27-29 May 2008, Perth, WA 14 Unfortunately, regardless of the good intentions of laboratory management, the incidence of poor sample preparation practices and unreported blank, duplicate and CRM failures is higher than expected or desired. Sole reliance on the internal laboratory QC is an unacceptably poor practice. Do We Need Blind Insertions? The identity and characteristics of the control samples must remain unknown to the controlled entity. Otherwise, the objectivity is lost, the control may no longer be valid, and can consequently be called Blind Insertions Sampling 2008, 27-29 May 2008, Perth, WA 15 the control may no longer be valid, and can consequently be called into question. The purpose of the blind insertion of control samples is to prevent the laboratory from identifying the control samples, or at the very least, their nature and sought values, so that an objective and independent assessment of precision, accuracy and contamination can be conducted. Are Blind Insertions Possible? Blind insertion of field duplicates and coarse blanks can be easily conducted at site, during the sampling process. Blind Insertions Sampling 2008, 27-29 May 2008, Perth, WA 16 Blind insertion of other control samples (same-batch preparation and pulp duplicates, CRMs, pulp blanks) would require insertion into the batches during or after sample preparation, and prior to assaying. Unless sample preparation and assaying take place at different laboratories or facilities, this operation would be impossible without the participation of non-laboratory personnel. Then, What About Sample Security? Under these conditions, samples would have to be temporarily returned to the custody of a non-laboratory person in charge of the insertions, even if this occurs within the laboratory premises. Sample Security Sampling 2008, 27-29 May 2008, Perth, WA 17 Is this an acceptable practice? Does it represent a breach in the Chain of Custody principle? If so, what do we give up? Proper assessment of precision, accuracy and contamination? Sample security and the Chain of Custody principle? Are those two alternatives compatible? Being in Custody A sample is considered to be in custody if it meets at least one of the following conditions: Sample Security Sampling 2008, 27-29 May 2008, Perth, WA 18 the following conditions: The sample is in someones physical possession or view; The sample is secured to prevent tampering; or The sample is secured in an area restricted to authorized personnel. (WSDE, 2007) Chain of Custody Chain of Custody is defined as "an unbroken trail of accountability that ensures the physical security of samples, data, and records Sample Security Sampling 2008, 27-29 May 2008, Perth, WA 19 that ensures the physical security of samples, data, and records (EPA, 1998). This definition has to do with secure traceability. According to this definition, respecting the chain of custody implies that it should be known and documented who has custody of a sample at any particular moment. As long as this principle is followed, the chain of custody concept is respected. Currently accepted situations when neither the company nor the laboratory are in permanent custody of the samples: Samples are taken on site, and submitted for preparation and assaying to another location (city, country or continent) by various means (horse, water Sample Security Sampling 2008, 27-29 May 2008, Perth, WA 20 another location (city, country or continent) by various means (horse, water buffalo, truck, bus, train, plane, mail or courier), using company personnel or contractors (individuals, same laboratory, another laboratory or other contractors). Samples are prepared on site by company personnel or by a special contractor or by laboratory personnel, and are submitted for assaying to another location (city, country or continent) by various means (horse, water buffalo, truck, bus, train, plane, mail or courier), using contractors (individuals, same laboratory, another laboratory or other contractors). Currently accepted situations when neither the company nor the laboratory are in permanent custody of the samples: Samples are prepared by a laboratory facility in one location and submitted for assaying to another facility of the same laboratory in the same location or Sample Security Sampling 2008, 27-29 May 2008, Perth, WA 21 for assaying to another facility of the same laboratory in the same location or in another location (city, country or continent) by various means (truck, bus, train, plane, mail or courier) using laboratory personnel or various contractors (individuals, laboratory, other contractors). Samples are prepared by a laboratory facility in one location and submitted for assaying to another facility of another laboratory in the same location or in another location (city, country or continent) by various means (truck, bus, train, plane, mail or courier) using laboratory personnel or various contractors. Therefore, in spite of the fact that potential tampering possibilities exist, such situations Sample Security Sampling 2008, 27-29 May 2008, Perth, WA 22 tampering possibilities exist, such situations (and others) are customarily accepted because changes of custody are well documented with Chain of Custody forms. Conditions for Blind Insertions The QP is entitled to follow or to accept practices based on criteria that are generally accepted by the industry, or that Quality Control versus Sample Security Sampling 2008, 27-29 May 2008, Perth, WA 23 criteria that are generally accepted by the industry, or that can reasonably be justified on scientific or technical grounds. The QC process should be sufficiently transparent to prevent any suspicion of improper behaviour or actions; an essential requirement is that the events should be adequately documented. When AMEC is retained by an exploration or mining company for the independent, ongoing review of a quality control program: A trained AMEC employee is in charge of the blind insertion of control samples at the laboratory premises, with AMECs Blind Insertion Practice Sampling 2008, 27-29 May 2008, Perth, WA 24 of control samples at the laboratory premises, with authorization of company and laboratory management; Control samples are repackaged in pouches identical to those used for unknown samples, supplied by the laboratory on the spot, and chain of custody forms are filled by the AMEC and the laboratory representatives at the time when sample custody changes. AMEC does not recommend nor accept that samples be retrieved from the laboratory premises before assaying for the insertion of blind control samples or for any other purpose. Using one laboratory (or branch) for preparation and insertion of the control samples, and another laboratory (or branch) for assaying. This procedure can be considered as best practice. Using trained personnel independent of the exploration or mining company, with no vested interest in the project, to do the blind Recommended Blind Insertion Procedures Sampling 2008, 27-29 May 2008, Perth, WA 25 company, with no vested interest in the project, to do the blind insertions within the laboratory premises. This process should be well documented with chain of custody forms. This procedure can be considered as best practice. Using a trained person from the company to do the blind insertions within the laboratory premises. The process should be well documented with chain of custody forms. This procedure can be considered as acceptable. Final Recommendations Implement from Day 1 a comprehensive QA/QC program. Sampling 2008, 27-29 May 2008, Perth, WA 26 program. Use same-batch duplicates. Use blind insertions. Keep proper records of changes of custody.
(AAPS Advances in the Pharmaceutical Sciences Series 21) Russell Weiner, Marian Kelley (eds.)-Translating Molecular Biomarkers into Clinical Assays _ Techniques and Applications-Springer Internation.pdf
(AAPS Advances in the Pharmaceutical Sciences Series 21) Russell Weiner, Marian Kelley (eds.)-Translating Molecular Biomarkers into Clinical Assays _ Techniques and Applications-Springer Internation.pdf