Download Guidance for the Implementation of a Quality Management by United Nations PDF

By United Nations

Deals suggestions for the implementation of a top quality administration approach in drug checking out laboratories: a dedication to caliber and non-stop development.

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Extra info for Guidance for the Implementation of a Quality Management System in Drug Testing Laboratories: A Commitment to Quality and Continuous Improvement (United Nations Office at Vienna)

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An expiry date furnished by a vendor/manufacturer determines the useful lifetime of the standard/reagent/material unless it can be verified beyond that date. Where ­appropriate, “opened” and “use by” dates should also be recorded. It is important to note that problems with standards and reagents can arise after they have been received in the laboratory. As soon as a container is opened there is a risk of it becoming contaminated or otherwise changing in composition. Bottles that are not tightly resealed expose their contents to air, with the possible loss or pick-up of moisture and absorption of carbon dioxide or other contaminating vapours.

11. 2. 12. a. 13. United Nations Office on Drugs and Crime, Staff Skill Requirements and Equipment Recommendations for Forensic Science Laboratories, 2009. 14. United Nations Office on Drugs and Crime, Validation of analytical methodology and calibration of equipment used for testing of illicit drugs in seized materials and biological specimen, 2009. 15. Eurachem, Quantifying Uncertainty in Analytical Measurement, 2nd Edition, 2000. 16. The International Narcotics Control Board (INCB), Guidelines for the import and export of drug and precursor reference standards, 2007.

The sampling plan and/or sampling procedure, the identification of the person taking the sample and the environmental conditions, if relevant, should be recorded. For sampling seized materials, the sampling plans and procedures published by internationally recognized organizations, such as UNODC [4], ENFSI [18] or SWGDRUG [5], are recommended. For sampling biological specimens, the sampling plans and procedures published by UNODC [4] or the European Guidelines for ­Workplace Drug Testing [8] are recommended.

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