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The technologies of this document specified are description languages and vocabularies to describe virtual world objects. The adaptation engine is not within the scope of this document. This document specifies syntax and...

This document defines a privacy architecture framework that: — specifies concerns for ICT systems that process PII; — lists components for the implementation of such systems; and — provides architectural views contextualizing...

This document specifies high efficiency video coding.

This document specifies mechanisms for the provision of specific, communication-related, non-repudiation services using asymmetric cryptographic techniques.

This document specifies technology for loudness and dynamic range control. It is applicable to most MPEG audio technologies. It offers flexible solutions to efficiently support the widespread demand for technologies such as...

This document specifies the architecture of MPEG-V (media context and control) and its three types of associated use cases: information adaptation from virtual world to real world; information adaptation from real world to...

This document specifies high efficiency video coding.

This part of ISO/IEC 15459 specifies the common rules applicable for unique identification that are required to ensure full compatibility across different identities.

This document specifies and publishes registered Common Biometric Exchange Formats Framework (CBEFF) patron formats defined by the CBEFF patron ISO/IEC JTC 1/SC 37, and specifies their registered CBEFF patron format types...

This part of ISO 500 gives general specifications, including speeds, safety requirements, the dimensions for master shield, and clearance zones for rear-mounted power take-offs (PTOs) of types 1, 2, 3, and 4 on agricultural...

The ISO 11607-1 specifies requirements and test methods for materials, preformed sterile barrier systems, sterile barrier systems and packaging systems that are intended to maintain sterility of terminally sterilized medical...

The ISO 11607-2 specifies requirements for the development and validation of processes for packaging medical devices that are terminally sterilized. These processes include forming, sealing and assembly of preformed sterile...