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17/30331313 DC : 0

NA

NA

Status of Standard is Unknown

BS EN ISO 20186-2 - MOLECULAR IN VITRO DIAGNOSTIC EXAMINATIONS - SPECIFICATIONS FOR PRE-EXAMINATION PROCESSES FOR VENOUS WHOLE BLOOD - PART 2: ISOLATED GENOMIC DNA CORRECT

Available format(s)

Hardcopy , PDF

Language(s)

English

£20.00
Excluding VAT

Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 General Considerations
5 Outside the laboratory
6 Inside the laboratory
Annex A (informative) - Impact of pre-examination
        process steps on venous whole blood genomic
        DNA quality
Bibliography

BS EN ISO 20186-2.

Committee
CH/212
DocumentType
Draft
Pages
29
PublisherName
British Standards Institution
Status
NA

ISO 22174:2005 Microbiology of food and animal feeding stuffs — Polymerase chain reaction (PCR) for the detection of food-borne pathogens — General requirements and definitions
CLSI MM19 A : 1ED 2011 ESTABLISHING MOLECULAR TESTING IN CLINICAL LABORATORY ENVIRONMENTS
ISO 18113-1:2009 In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements
ISO/TS 17822-1:2014 In vitro diagnostic test systems Qualitative nucleic acid-based in vitro examination procedures for detection and identification of microbial pathogens Part 1: General requirements, terms and definitions
ISO 15189:2012 Medical laboratories — Requirements for quality and competence
ISO 17511:2003 In vitro diagnostic medical devices Measurement of quantities in biological samples Metrological traceability of values assigned to calibrators and control materials
ISO 15190:2003 Medical laboratories Requirements for safety
ISO/IEC 17043:2010 Conformity assessment — General requirements for proficiency testing
ISO Guide 30:2015 Reference materials — Selected terms and definitions
ISO 9000:2015 Quality management systems — Fundamentals and vocabulary

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