Systems and software engineering — Software life cycle processes
This National Standard of Canada is equivalent to International Standard ISO/IEC 12207:2008.
1.1 Scope
This International Standard establishes a common framework for software life cycle processes, with welldefined
terminology, that can be referenced by the software industry. It contains processes, activities, and
tasks that are to be applied during the acquisition of a software product or…
Anaesthetic and Respiratory Equipment - Laryngoscopes for Tracheal Intubation
This National Standard of Canada is based on International Standard ISO 7376:2003.
1 Scope
This International Standard specifies general requirements for laryngoscopes and critical dimensions for the handle and lamp of hook-on type laryngoscopes.
It is applicable only to instruments with an electrical power source for illuminating the larynx, since electrical safety requirements may be more…
Medical Electrical Equipment - Particular Requirements for the Basic Safety and Essential Performanc...
This National Standard of Canada is equivalent to International Standard ISO 21647:2004, including Technical Corrigendum 1:2005.
1* Scope
IEC 60601-1:1998, Clause 1, applies, except as follows.
Amendment (add at the end of 1.1):
This International Standard specifies particular requirements for the basic safety and essential performance of respiratory gas monitors (RGM) (as defined in 3.15)…
Environmental Management - Life Cycle Assessment - Principles and Framework
This National Standard of Canada is equivalent to International Standard ISO 14040:2006.
1 Scope
This International Standard describes the principles and framework for life cycle assessment (LCA) including
a) the goal and scope definition of the LCA,
b) the life cycle inventory analysis (LCI) phase,
c) the life cycle impact assessment (LCIA) phase,
d) the life cycle interpretation phase…
Information Technology - Open Systems Interconnection - Session Service Definition
This National Standard of Canada is equivalent to International Standard ISO/IEC 8326:1996 (second edition, 1996-09-15).
1 Scope
This Recommendation / International Standard defines in an abstract way the externally visible service provided by the OS1 Session Layer in terms of:
a) the primitive actions and events of the service;
b) the parameter data associated with each primitive…
Nomenclature - Specification for a Nomenclature System for Medical Devices for
the Purpose of Regul...
This National Standard of Canada is equivalent to International Standard ISO
15225:2000.
1 Scope
This European Standard specifies requirements and guidance for the construction
of a nomenclature for medical devices in order to facilitate co-operation and
exchange of regulatory data on an international level between interested
parties such as: Regulatory Authorities, Manufacturers,…
Quality systems - Medical devices - Particular requirements for the application of ISO 9001
This National Standard of Canada is equivalent to International Standard ISO 13485:1996.
1 Scope
This International Standard specifies, in conjunction with ISO 9001, the
quality system requirements for the design/development, production and, when
relevant, installation and servicing of medical devices.
This International Standard, in conjunction with ISO 9001, is applicable when…
Quality systems - Medical devices - Particular requirements for the application
of ISO 9002
This National Standard of Canada is equivalent to International Standard ISO
13488:1996.
1 Scope
This International Standard specifies, in conjunction with IS0 9002, the
quality system requirements for the production and, when relevant, installation
and servicing of medical devices.
This International Standard, in conjunction with ISO 9002, is applicable when
there is a need to…
Quality management - Guidelines for configuration management
This National Standard of Canada is equivalent to International Standard ISo
10007:1995.
1 Scope
This International Standard gives guidance on the use of configuration
management in industry and its interface with other management systems and
procedures. It first provides a management overview (clause 4), then describes
the process, organization and detailed procedures.
It is…
1.1 These requirements cover the design and construction of Type L vents intended for the venting of
flue gases having temperatures not exceeding 300 °C, from fuel-burning appliances certified for use with
Type L vents. The vents may also be used where Type B gas vents are used. They are intended for
installation in buildings to provide a passageway for conveying flue gases to the outer air…