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Guidance for Preparing Standard Operating Procedures (SOPs)

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Data ML005<br />

Rev. # 0.0<br />

Date: 11/00<br />

Page 3 of 16<br />

1. Purpose:<br />

The purpose of this standard operating procedure is to ensure that all reviews of analyses<br />

<strong>for</strong> metals in environmental samples are of similar quality. Raw data review is a very critical part<br />

of the analytical process. A thorough review can prevent errors in reporting or shortcuts in<br />

procedure on the part of the analyst. It is imperative that a thorough review be conducted because<br />

some of the data may be used as evidence in court proceedings. Raw data review is also needed<br />

to ensure that the acceptance criteria <strong>for</strong> the project have been met.<br />

2. Applicability:<br />

All data produced by the Region 11 laboratory must be reviewed be<strong>for</strong>e its release to the<br />

client. Data produced in the analysis of metals must be reviewed by the procedure described<br />

herein.<br />

3. Procedure Summary:<br />

3.1 There are three levels of data review. These are done by the analyst, a peer, and<br />

the quality control (QC) coordinator. The analyst and peer do similar depth of<br />

profile review, while the QC coordinator does an in-depth review, on an as-needed<br />

basis. This would be done as a random spot-check, or selectively, as in the case of<br />

a high profile survey. There are three types of review <strong>for</strong> the analyst and peer.<br />

These are Package Overview, determining correctness of the reports and<br />

completeness of the package (Section 5); Quality Control Review, determining the<br />

quality of the data from the audits (Section 6); and Technical Review, determining<br />

that the data are not compromised by matrix effects (Section 7). The QC<br />

coordinator will do all of these, plus examine the electronic records.<br />

3.2 A narrative prepared by the analyst is included with the data (Section 9). This<br />

document contains a description of the samples, the purpose of the analysis<br />

(acceptance criteria, if known), all operations with the samples, including<br />

corrective actions taken in the process, the filenames and paths <strong>for</strong> all electronic<br />

records pertaining to the analysis, and the result of the analyst’s QC review with<br />

comments about the usability of the data.<br />

3.3 Each reviewer is responsible <strong>for</strong> verifying each of the parts that are designated <strong>for</strong><br />

their review and <strong>for</strong> completing the checklist (Attachment 1) associated with the<br />

data package.<br />

QA/G-6 E-3<br />

March 2001

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