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The primary purpose of the multipart standard ISO/IEC 19763 is to specify a metamodel framework for interoperability. ISO/IEC 19763-5:2015 specifies the metamodel that describes a facility to register administrative...

This Standard defines the architectural elements of the Trusted Platform Module (TPM), a device which enables trust in computing platforms in general. Some TPM concepts are explained adequately in the context of the TPM...

This Standard contains C code that describes the algorithms and methods used by the command code in ISO/IEC 11889-3. The code in ISO/IEC 11889-4:2015 augments ISO/IEC 11889-2 and ISO/IEC 11889-3 to provide a complete...

This Standard specifies the properties of Base Functional Specification View (FSV) Standards in order to best meet the requirements of the Business Operational View (BOV) with interoperable implementations. Base FSV standards...

This service definition is compliant with the UPnP Device Architecture version 1.0 . This service type enables control over the transport of audio and video streams. The service type defines a ?common' model for A/V transport...

This Standard provides requirements and guidelines for preventing the unauthorized modification of Basic Input/Output System (BIOS) firmware on PC client systems. Unauthorized modification of BIOS firmware by malicious...

This Standard defines the crypto suite for ECC-DH for the ISO/IEC 18000 air interfaces standards for radio frequency identification (RFID) devices. Its purpose is to provide a common crypto suite with Diffie-Hellmann-based...

This Standard defines the crypto suite for AES 128 for the ISO/IEC 18000 air interfaces standards for radio frequency identification (RFID) devices. Its purpose is to provide a common crypto suite for security for RFID...

This Standard defines the Crypto Suite for Grain-128A for the ISO/IEC 18000 air interface standards for radio frequency identification (RFID) devices. Its purpose is to provide a common crypto suite for security for RFID...

This standard specifies the information to be provided by the medical device manufacturer on the processing of medical devices claimed to be re-sterilizable and medical devices intended to be sterilized by the processor. This...

1.1 General 1.1.1 This part of ISO 11138 provides general requirements for production, labelling, test methods and performance characteristics of biological indicators, including inoculated carriers and suspensions, and their...

1.1 This Standard provides performance requirements and test methods for evaluating power consumption of internally lighted exit signs. Note: Visibility requirements are contained in CSA C22.2 No. 141. 1.2 Exit signs...