ГОСТ Р 59787—2021
Библиография
[1JISO 15189:2012. Medical laboratories — Requirements for quality and competence (
Л
аборатории медицинские.
Частные требования к качеству и компетентности)
(2)ISO 9000:2015. Quality management systems — Fundamentals and vocabulary (Системы менеджмента каче
ства. Основные положения и словарь)
(3)ISO 9001, Quality management systems — Requirements (Системы менеджмента качества. Требования)
(4) ISO 15190:2003. Medical laboratories — Requirements for safety (Медицинские лаборатории. Требования без
опасности)
(5) CSA Z316.7—12. Primary sample collection facilities and medical laboratories — Patient safety and quality of care
— Requirements for collecting, transporting, and storing samples
(6) CDC. Good Laboratory Practices for Molecular Genetic Testing for Heritable Diseases and Conditions. MMWR R&R,
June 12. 2009. Vol 58. N0. RR-6
(7)CDC. Guideline for Disinfection and Sterilization in Healthcare Facilities. Rutala W.A.. Weber D.J. 2008
(8)CLSI. Accuracy in Patient and Sample Identification; Approved Guideline. CLSI document GP33-A. Clinical and
Laboratory Standards Institute. Wayne. PA. 2010
(9)CLSI. Collection. Transport. Preparation, and Storage of Specimens for Molecular Methods; Approved Guideline.
CLSI document MM13-A. Clinical and Laboratory Standards Institute. Wayne. PA. 2005
(10) CLSI. Procedures and Devices for the Collection of Diagnostic Capillary Blood Specimens; Approved Standard —
Sixth Edition. CLSI document GP42-A6. Clinical and Laboratory Standards Institute. Wayne. PA. 2008
(11) CLSI. Procedures for the Collection of Diagnostic BJood Specimens by Venipuncture; Approved Standard — Sixth
Edition. CLSI document GP41-A6. Clinical and Laboratory Standards Institute. Wayne. PA. 2007
(12) CLSI. Procedures for the Handling and Processing of Blood Specimens for Common Laboratory Tests; Approved
Guideline — Fourth Edition. CLSI document GP44-A4. Clinical and Laboratory Standards Institute. Wayne. PA. 2010
(13) CLSI. Quality Management for Molecular Genetic Testing: Approved Guideline CLSI document MM20-A. Clinical
and Laboratory Standards Institute. Wayne. PA. 2012
(14) Howie S.R.C. Blood sample volumes in child health research: Review of safe limits. Bulletin of the World Health
Organization Published online. September 2010
(15) Lindbtad B.. & Alstrom T. Recommendation for collection of venous blood from children, with special reference to
production reference values. Scand. J. Clin. Lab. Invest. 1990. 50 pp. 99—104
(16) Lippi G.. & Becan-McBride K. Preanalytical quality improvement: in quality we trust. Clin. Chem. Lab. Med. 2013,
51 (1) pp. 229—241
(17) Miller M.. Bachorik P.S.. Cloey T.A. Normal Variation of Plasma Lipoproteins: Postural Effects on Plasma
Concentrations of Lipids. Lipoproteins, andApolipoproteins. Clin. Chem. 1992. 38 (4) pp. 569—574
(18) Miller W.G.. & Tate J.R. Harmonization: the Sample, the Measurement, and the Report Ann. Lab. Med. 2014. 34
pp. 187—197
(19) Ontario Agency for Health Protection and Promotion. Provincial Infectious Diseases Advisory Committee. Best
Practices for Environmental Cleaning for Prevention and Control of Infections in All Health Care Settings. 2nd
Revision. Queen’s Printer for Ontario, Toronto. ON. 2012
(20) Plebani M. Quality indicators to detect pre-analytical errors in laboratory testing. Clin. Biochem. Rev. 2012. 33 pp.
85—88
(21) Raffick A.R.. Bowen A., Remaley T. Interferences from blood collection tube components on clinical chemistry
assays. Biochem. Med. 2014. 24 (1) pp. 31—44
(22) Sztefko K.. & Beba J. Blood loss from laboratory diagnostic tests in children. Clin. Chem. Lab. Med. 2013. 51 (8) pp.
1623—1626
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