CSA Z15190 : 2005 : R2015
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by
MEDICAL LABORATORIES - REQUIREMENTS FOR SAFETY
Hardcopy , PDF
16-09-2020
English
01-01-2015
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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Superseded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 | |
| Supersedes |
| 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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