00/560160 DC : DRAFT JAN 2000
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
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BS ISO 15197 DETERMINATION OF PERFORMANCE CRITERIA FOR IN VITRO BLOOD GLUCOSE MONITORING SYSTEMS FOR MANAGEMENT OF HUMAN DIABETES MELLITUS
27-05-2003
23-11-2012
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Design
4.1 Ergonomic/human factor aspects
4.2 Risk analysis
5 Labelling and documentation
5.1 Blood glucose monitor labels
5.2 User manual for the blood glucose monitoring
system
5.3 Reagent system and control material labels
5.4 Reagents and control material inserts
6 Blood glucose monitor design and interference
aspects
6.1 Protection against electric shock and patient
leakage current
6.2 Protection against mechanical hazards
6.3 Baseline performance test
6.4 Mechanical resistance to shock, vibration,
and impact
6.4.1 Vibration test protocol
6.4.2 Drop test protocol
6.5 Equipment humidity exposure test protocol
6.5.1 High temperature test protocol
6.5.2 Low temperature test protocol
6.6 Resistance to heat
6.7 Resistance to moisture and liquids
6.8 Protection against liberated gases, explosion,
and implosion
6.9 Components
6.10 Equipment humidity exposure test protocol
7 Technical performance evaluation
7.1 Imprecision testing
7.1.1 General
7.1.2 Within run imprecision test protocol
7.1.3 Total imprecision (day-to-day) test
7.1.4 Data presentation
7.2 Accuracy testing
7.2.1 General
7.2.2 Materials/Methods
7.2.3 Run format
7.2.4 Data presentation
7.3 Minimum acceptable performance
8 User performance evaluation
8.1 Selection of user groups
8.2 Selection of evaluation sites
8.3 User instructions
8.4 User techniques
Annex A (informative) Analytical Performance
Requirements for Self-Monitoring of
Blood Glucose for the Contro of Diabetes
Mellitus
A.1 Purpose
A.2 Introduction
A.3 Currently Accepted Performance Criteria
A.4 Current state-of-the-art
A.5 Clinical Studies
A.6 Conclusions
Bibliography
Committee |
CH/69
|
DocumentType |
Draft
|
PublisherName |
British Standards Institution
|
Status |
Superseded
|
SupersededBy |
CSA Z316.4 : 0 | PERFORMANCE SPECIFICATIONS FOR PORTABLE WHOLE BLOOD GLUCOSE MONITOR SYSTEMS FOR USE IN DIABETES MANAGEMENT |
EN 592 : 2002 | INSTRUCTIONS FOR USE FOR IN VITRO DIAGNOSTIC INSTRUMENTS FOR SELF-TESTING |
EN 376 : 2002 | INFORMATION SUPPLIED BY THE MANUFACTURER WITH IN VITRO DIAGNOSTIC REAGENTS FOR SELF-TESTING |
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 14971-1:1998 | Medical devices Risk management Part 1: Application of risk analysis |
IEC 61010-1:2010+AMD1:2016 CSV | Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 1: General requirements |
ISO 3534-1:2006 | Statistics — Vocabulary and symbols — Part 1: General statistical terms and terms used in probability |
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