Comment Closes On
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|
Committee
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CH/62/1 |
Document Type
|
Draft |
ISBN
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|
Pages
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Published
|
|
Publisher
|
British Standards Institution
|
Status
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Superseded |
Superseded By
|
|
IEC GUIDE 109:2012
|
Environmental aspects - Inclusion in electrotechnical product standards |
IEC 60050-351:2013
|
International Electrotechnical Vocabulary (IEV) - Part 351: Control technology |
IEC 60601-1:2005+AMD1:2012 CSV
|
Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
IEC 60601-1-6:2010+AMD1:2013 CSV
|
Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability |
ISO 14021:2016
|
Environmental labels and declarations — Self-declared environmental claims (Type II environmental labelling) |
IEC 60601-1-8:2006+AMD1:2012 CSV
|
Medical electrical equipment - Part 1-8: General requirements forbasic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems inmedical electrical equipment and medical electrical systems |
ISO/IEC Guide 51:2014
|
Safety aspects Guidelines for their inclusion in standards |
IEC 62304:2006+AMD1:2015 CSV
|
Medical device software - Software life cycle processes |
ISO/TR 14062:2002
|
Environmental management Integrating environmental aspects into product design and development |
ISO 14001:2015
|
Environmental management systems — Requirements with guidance for use |
ISO 9000:2015
|
Quality management systems — Fundamentals and vocabulary |
ISO 14971:2007
|
Medical devices Application of risk management to medical devices |
ISO 14040:2006
|
Environmental management Life cycle assessment Principles and framework |
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