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CSA Z15190 : 2005

Superseded
Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

View Superseded by
superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

MEDICAL LABORATORIES - REQUIREMENTS FOR SAFETY
Available format(s)

Hardcopy , PDF

Superseded date

19-07-2021

Language(s)

English

Published date

01-01-2015

Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Risk group classification
5 Management requirements
6 Designing for safety
7 Staffing, procedures, documentation, inspection and
   records
8 Identification of hazards
9 Reporting of incidents, injury, accidents and
   occupational illnesses
10 Training
11 Personnel responsibilities
12 Clothing and personal protective equipment (PPE),
   including gloves, eye, face, foot and
   respiratory protection
13 Good housekeeping practices
14 Safe work practices
15 Aerosols
16 Microbiological safety cabinets, chemical safety hoods
   and cabinets
17 Chemical safety
18 Radiation safety
19 Fire precautions
20 Emergency evacuations
21 Electrical equipment
22 Transport of samples
23 Waste disposal
Annex A (informative) - Action-plan outline for implementation
        of this International Standard
Annex B (informative) - Laboratory safety audit
Annex C (informative) - Decontamination, cleaning and
        disinfection following a spillage
Bibliography

Defines requirements for safe practices in the medical laboratory.

DocumentType
Standard
Pages
56
ProductNote
Reconfirmed EN
PublisherName
Canadian Standards Association
Status
Superseded
SupersededBy

IEC 61010-2-051:2015 Safety requirements for electrical equipment for measurement, control and laboratory use - Part 2-051: Particular requirements for laboratory equipment for mixing and stirring
BS 8800:1996 Guide to occupational health and safety management systems
EN 13641:2002 Elimination or reduction of risk of infection related to in vitro diagnostic reagents
IEC TR 61010-3-051:1999 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 3-051: Conformity verification report for IEC 61010-2-051, Particular requirements for laboratory equipment for mixing and stirring
CLSI M29 A2 : 2ED 2001 PROTECTION OF LABORATORY WORKERS FROM OCCUPATIONALLY ACQUIRED INFECTIONS
ISO 15189:2012 Medical laboratories — Requirements for quality and competence
IEC 61010-2-032:2012 Safety requirements for electrical equipment for measurement, control and laboratory use - Part 2-032: Particular requirements for hand-held and hand-manipulated current sensors for electrical test and measurement
BS 7179-1:1990 Ergonomics of design and use of visual display terminals (VDTs) in offices Introduction
ISO/IEC Guide 63:2012 Guide to the development and inclusion of safety aspects in International Standards for medical devices
IEC TR 61010-3-010:1999 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 3-010: Conformity verification report for IEC 61010-2-010, Particular requirements for laboratory equipment for the heating of materials
ISO/IEC Guide 51:2014 Safety aspects Guidelines for their inclusion in standards
IEC TR 61010-3-061:1999 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 3-061: Conformity verification report for IEC 61010-2-061, Particular requirements for laboratory atomic spectrometers with thermal atomization and ionization
BS 6324-1:1983 Terms relating to surgical implants Glossary of general medical terms
IEC 61010-2-045:2000 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-045: Particular requirements for washer disinfectors used in medical, pharmaceutical, veterinary and laboratory fields
IEC 61010-2-041:1995 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-041: Particular requirements for autoclaves using steam for the treatment of medical materials, and for laboratory processes
IEC 61010-2-020:2016 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-020: Particular requirements for laboratory centrifuges
IEC 61010-2-043:1997 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-043: Particular requirements for dry heat sterilizers using either hot air or hot inert gas for the treatment of medical materials, and for laboratory processes
IEC 61010-031:2015 RLV Safety requirements for electrical equipment for measurement, control and laboratory use - Part 031: Safety requirements for hand-held probe assemblies for electrical measurement and test
IEC 61010-2-010:2014 Safety requirements for electrical equipment for measurement, control and laboratory use - Part 2-010: Particular requirements for laboratory equipment for the heating of materials
CLSI GP5 A : 1993 CLINICAL LABORATORY WASTE MANAGEMENT<br>
EN 12469:2000 Biotechnology - Performance criteria for microbiological safety cabinets
IEC 61010-2-061:2015 Safety requirements for electrical equipment for measurement, control and laboratory use - Part 2-061: Particular requirements for laboratory atomic spectrometers with thermal atomization and ionization
IEC 61010-1:2010+AMD1:2016 CSV Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 1: General requirements
IEC 61010-2-042:1997 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-042: Particular requirements for autoclaves and sterilizers using toxic gas for the treatment of medical materials, and for laboratory processes
CLSI GP17 A : 1ED 96 CLINICAL LABORATORY SAFETY
IEC TR 61010-3-020:1999 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 3-020: Conformity verification report for IEC 61010-2-020:1992 Particular requirements for laboratory centrifuges

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