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The scope of IEC 61730-1 is also applicable to this part of IEC 61730. While IEC 61730-1 outlines the requirements of construction, this part of the standard lists the tests a PV module is required to fulfill for safety...

1.1 Inclusions 1.1.1 This International Standard specifies general requirements for the characterization of a sterilizing agent and for the development, validation and routine monitoring and control of a sterilization process...

Scope: The proposed standard will establish a glossary of terms and definitions on low carbon construction along the full life cycle of construction, applicable to both operational and embodied carbon emission reductions. The...

1.1 This standard provides the requirements for modular built relocatable temporary structures. 1.2 Relocatable structures for temporary use are a form of modular construction, built in an approved offsite facility, designed...

1.1 This Standard applies to 60 to 250 °C single- or multiple-conductor, jacketed or unjacketed, integral or non-integral cables and single or multiple coaxial cables for telephone and other communication circuits such as...

Note: The standard development activity of this Notice of Intent (originally published on June 4, 2024) was updated by the responsible SDO on September 4, 2024. 1.1 This Standard applies to Class A, single- and three-phase...

This National Standard of Canada applies to two types of automotive fuel: type 1, 50% to 85% by volume denatured fuel ethanol with gasoline and type 2, 20% to 25% by volume denatured fuel ethanol with gasoline. Both types are...

1.1 This part of ISO 11137 specifies requirements for the development, validation and routine control of a radiation sterilization process for medical devices. NOTE Although the scope of this part of ISO 11137 is limited to...

Note: The project need for this NOI (originally published on November 2, 2021) was updated by the responsible SDO on December 21, 2021. Scope of UL/ULC 2200: These requirements cover stationary engine generator assemblies...

1.1 This part of ISO 11137 specifies requirements for the development, validation and routine control of a radiation sterilization process for medical devices. NOTE Although the scope of this part of ISO 11137 is limited to...