ASTM International - ASTM E2327-04
Standard Practice for Quality Assurance of Laboratories Performing Seized-Drug Analysis
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| Organization: | ASTM International |
| Publication Date: | 1 October 2004 |
| Status: | inactive |
| Page Count: | 5 |
| ICS Code (Analytical chemistry in general): | 71.040.01 |
significance And Use:
These are minimum standards of quality assurance applicable to laboratories where analysis of seized-drug submissions is performed.
The standards are to be practiced by forensic analysts... View More
scope:
1.1 This standard covers quality assurance issues in forensic laboratories performing seized-drug analysis including evidence handling, analytical procedures, report writing, method validation, documentation, proficiency testing, audits, and health and safety.
1.2 Standards are meant to apply only to the practice of qualitative seized-drug analysis.
Document History
May 1, 2015
Standard Practice for Quality Assurance of Laboratories Performing Seized-Drug Analysis
1.1 This practice covers quality assurance issues in forensic laboratories performing seized-drug analysis including evidence handling, analytical procedures, report writing, method validation,...
May 1, 2015
Standard Practice for Quality Assurance of Laboratories Performing Seized-Drug Analysis
1.1 This practice covers quality assurance issues in forensic laboratories performing seized-drug analysis including evidence handling, analytical procedures, report writing, method validation,...
December 15, 2010
Standard Practice for Quality Assurance of Laboratories Performing Seized-Drug Analysis
1.1 This practice covers quality assurance issues in forensic laboratories performing seized-drug analysis including evidence handling, analytical procedures, report writing, method validation,...
ASTM E2327-04
October 1, 2004
Standard Practice for Quality Assurance of Laboratories Performing Seized-Drug Analysis
1.1 This standard covers quality assurance issues in forensic laboratories performing seized-drug analysis including evidence handling, analytical procedures, report writing, method validation,...