ASTM-E2549 › Standard Practice for Validation of Seized-Drug Analytical Methods (Withdrawn 2023)
The following bibliographic material is provided to assist you with your purchasing decision:
Scope
1.1 This practice addresses the validation of qualitative and quantitative seized-drug analytical methods. It discusses the validation of analytical methods in terms of their part in analytical schemes and in terms of performance characteristics including brief mention of measurement uncertainty and quality control parameters.
1.2 This practice does not replace knowledge, skill, ability, experience, education or training and should be used in conjunction with professional judgment.
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.
Significance and Use
3.1 Validation is the confirmation by examination and the provision of objective evidence that the particular requirements for a specific intended use are fulfilled. There are numerous documents that address the topic of validation but there are few validation protocols for methods specific to seized drug analysis. This practice makes recommendations for the validation of both qualitative and quantitative methods used for the analysis of seized drugs.
Keywords
analytical scheme; methods; performance characteristics; seized-drug analytics; validation
To find similar documents by ASTM Volume:
To find similar documents by classification:
11.100.01 (Laboratory medicine in general)
This document comes with our free Notification Service, good for the life of the document.
This document is available in either Paper or PDF format.
Document Number
ASTM-E2549-14
Revision Level
2014 EDITION
Status
Cancelled
Modification Type
Withdrawn
Publication Date
March 15, 2014
Document Type
Practice
Page Count
3 pages
Committee Number
E30.11