Information technology - Media context and control - Part 6: Common types and tools
ISO/IEC 23005-6:2013 specifies syntax and semantics of the data types and tools common to the tools defined in the other parts of ISO/IEC 23005, such as basic data types which are used as basic building blocks in more than one of the tools in ISO/IEC 23005, colour-related basic types which are used in light and colour‑related tools to help in specifying colour-related characteristics of the…
Application integration at electric utilities - System interfaces for distribution management - Part...
IEC 61968-11:2013 specifies the distribution extensions of the common information model (CIM) specified in IEC 61970-301. It defines a standard set of extensions of common information model (CIM), which support message definitions in IEC 61968-3 to IEC 61968-9, IEC 61968-13 and IEC 61968-14. The scope of this standard is the information model that extends the base CIM for the needs of…
Fibre optic interconnecting devices and passive components - Performance standard - Part 089-2: Non-...
IEC 61753-089-2:2013 contains the minimum initial performance, test and measurement requirements and severities which a fibre optic pigtailed wide wavelength division multiplexing (WWDM) device for monitoring passive optical networks (PON) using an optical time-domain reflectometer (OTDR) satisfies in order to be categorized as meeting the requirements of category C (controlled environments), as…
Fibre optic interconnecting devices and passive components - Performance standard - Part 089-2: Non-...
IEC 61753-089-2:2013 contains the minimum initial performance, test and measurement requirements and severities which a fibre optic pigtailed wide wavelength division multiplexing (WWDM) device for monitoring passive optical networks (PON) using an optical time-domain reflectometer (OTDR) satisfies in order to be categorized as meeting the requirements of category C (controlled environments), as…
Cardiovascular implants — Cardiac valve prostheses — Part 3: Heart valve substitutes implanted by tr...
ISO 5840-3:2013 outlines an approach for verifying/validating the design and manufacture of a transcatheter heart valve substitute through risk management. The selection of appropriate verification/validation tests and methods are to be derived from the risk assessment. The tests may include those to assess the physical, chemical, biological and mechanical properties of heart valve substitutes…
Information technology — Telecommunications and information exchange between systems — Web Services ...
Web Services Description Language (WSDL) is an XML schema for describing Web services and how they can be accessed by Web based applications. WSDL facilitates the creation and deployment of web based applications. For example, by using WSDL with many industry Web services development environments, a web services developer can access features provided by an implementation without knowing details…
Information technology - Telecommunications and information exchange between systems - Web Services ...
Web Services Description Language (WSDL) is an XML schema for describing Web services and how they can be accessed by Web based applications. WSDL facilitates the creation and deployment of web based applications. For example, by using WSDL with many industry Web services development environments, a web services developer can access features provided by an implementation without knowing details…
Performance testing of nuclear air-cleaning systems at nuclear facilities
Scope
1.1 Facilities
1.1.1 Types of facilities
1.1.1.1 Class I nuclear facilities
This Standard addresses the design and execution of a nuclear air- cleaning system testing program for Class I nuclear facilities. These facilities include
a) nuclear reactors;
b) uranium fuel fabrication plants;
c) isotope processing facilities;
d) particle accelerators with a beam energy equal to or…
Scope
1.1 General
This Standard specifies requirements for the safe use, disinfection, testing, and maintenance of monitoring systems for hemodialysis. It is intended for use by dialysis providers, including health care workers and professionals who perform technical and operational functions associated with hemodialysis. This Standard applies to
a) quality management;
b) monitoring of fluid…
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…
