Medical device reprocessing - General requirements
Scope
1.1
This Standard is intended to form the basis of a QMS within a health care setting for the purpose of providing safe, reliable reprocessing of reusable medical devices and is designed to be used with the CSA Z314 series of Standards addressing specific aspects of medical device reprocessing.
A comprehensive QMS can be achieved when this Standard is used in combination with related…
Plume scavenging in surgical, diagnostic, therapeutic, and aesthetic settings
Scope
1.1
This Standard applies to systems and equipment used to capture and evacuate plume. It applies to all settings where such systems and equipment are used, including, but not limited to, the following:
a) surgical facilities;
b) dental clinics;
c) medical offices;
d) veterinary facilities;
e) laboratories and other research and testing facilities;
f) cosmetic…
1.1
This Standard addresses issues related to the safety of human perfusable organs used for transplantation. It includes quality system requirements and aspects of safety for potential and actual donors and recipients, personnel, and others who might be exposed to, or affected by, the transplantation of perfusable organs.
1.2
This Standard applies to establishments (or facilities) and…
Software Engineering - Product Quality - Part 4: Quality in Use Metrics
CSA Preface
Standards development within the Information Technology sector is harmonized with international standards development. Through the CSA Technical Committee on Information Technology (TCIT), Canadians serve as the Canadian Advisory Committee (CAC) on ISO/IEC Joint Technical Committee 1 on Information Technology (ISO/IEC JTC1) for the Standards Council of Canada (SCC), the ISO member…
Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-0...
This National Standard of Canada is based on International Standard IEC 1010-2-010:1992.
1. Scope and Object
This clause of Part 1 is applicable except as follows:
1.1 Scope:
This part 2 applies only to electrical powered laboratory equipment for the heating of materials, where the heating of materials is the only function or is one of several functions of the equipment.
1.1.2…
Safety Requirements for Electrical Equipment for Measurement, Control, and Laboratory Use - Part 2-0...
This National Standard of Canada is equivalent to International Standard IEC 61010-2-010:2003, second edition, 2003.
1 Scope and object
This clause of Part 1 is applicable except as follows:
1.1.1 Equipment included in scope Replacement:
Replace the text by the following: This part of IEC 61010 applies only to electrically powered laboratory equipment for the heating of materials, where the…
Requirements for the collection and transport of samples for medical laboratory examinations
Scope
This document specifies requirements and good practice recommendations for the collection and transport of samples intended for medical laboratory examinations.
This document is applicable to medical laboratories and service providers, which can be independent from the medical laboratory, involved in laboratory pre-examination processes that include the examination request, patient…
1 Scope
1.1
This Standard sets forth characteristics of effective and durable installation methods, in both new and existing buildings, of fenestration products within the scope of AAMA/WDMA/CSA 101/I.S.2/A440 that are intended for installation in buildings of all occupancies to which NBC Parts 3, 4, 5, and 6 of Division B apply.
1.2
In addition to fenestration products within the scope of…
1 Scope
1.1 Purpose
This Standard addresses issues related to the safety of human perfusable organs used for transplantation. It includes quality system requirements and aspects of safety for potential and actual donors and recipients, personnel, and others who might be exposed to, or affected by, the transplantation of perfusable organs.
1.2 Areas of application
This Standard applies to…