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1992-04-01_REVISION - M1988112
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1992-04-01_REVISION - M1988112
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Entry Properties
Last modified
6/19/2021 3:50:24 PM
Creation date
11/21/2007 11:05:44 PM
Metadata
Fields
Template:
DRMS Permit Index
Permit No
M1988112
IBM Index Class Name
Revision
Doc Date
4/1/1992
Doc Name
QUALITY ASSURANCE QUALITY CONTROL PROTOCOLS FOR THE COLLECTION OF SURFACE & GROUND WATER QUALITY
Type & Sequence
TR6
Media Type
D
Archive
No
Tags
DRMS Re-OCR
Description:
Signifies Re-OCR Process Performed
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' CORE LABOF,~ATORIES <br />~ ~/!/~ <br />Western Atlas <br />InterPational <br />~ ' TiTIE <br />' ANALYTICAL CHEMISTRY DIVISION QUALITY ASSURANCE MANUAL <br />' SOP N0. REVISION NO. EFFECTIVE DATE PAGiE <br />HC-QAC-02 0 1 /06/92 87 of 104 <br />' <br /> Units must be entered correctly (mg/L vs. mg/Kg, etc.) according to the <br /> sample matrix. Verify and change units in LIMS, if necessary, during data <br />' entry. <br /> Date/Time Analyzed <br /> Date-analyzed values which are entered in LIMS must accurately reflect the <br />' actual date of sample analysis. Enter the date and time when the analysis <br />began <br />not the ending date and time <br /> , <br />. <br /> Multiple QA numbers with different date/time analyzed val~yes are necessary <br /> to correctly enter a large group of samples processed over Several days (i.e., <br /> a single job which was processed in several different analytical batches. <br />' Quality Assurance Requirements <br /> Quality assurance data which is associated with an analytical batch must be <br /> entered into LIMS along with analytical results. If the qualify control sample <br /> checks are out of control and cannot be entered in LIMS (password override <br /> is required, analysts must immediately contact the appropriate laboratory <br /> section supervisor or the QA1QC coordinator for data valid$tion. <br />' 14.3 Data Review And Validation Process <br /> Group leaders and supervisors are responsible for verifying the analytical and <br />' quality control data generated in their laboratory section. Th@ following items <br /> must be reviewed and validated before releasing the data fdr final reporting. <br /> • Assure that the analytical method requirements were mgt during sample <br /> analysis. ~ <br /> • Verify that the analytical methodology which was used met the client's and <br /> regulatory requirements. I <br /> • Verify that quality control sample checks were analyzetl at the proper <br /> frequency and that quality control sample performance criteria were met. ' <br /> <br /> <br />
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