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The software release life cycle is the process of developing, testing, and distributing a software product (e.g., an operating system). It typically consists of several stages, such as pre-alpha, alpha, beta, and release candidate, before the final version, or "gold", is released to the public. An example of a basic software release life cycle
Release management is the process of managing, planning, scheduling and controlling a software build through different stages and environments; it includes testing and deploying software releases. [ 1 ] [ 2 ]
A relatively common practice is to make major jumps in version numbers for marketing reasons. Sometimes software vendors just bypass the 1.0 release or quickly release a release with a subsequent version number because 1.0 software is considered by many customers too immature to trust with production deployments.
IEC 62304 – medical device software – software life cycle processes [1] is an international standard published by the International Electrotechnical Commission (IEC). The standard specifies life cycle requirements for the development of medical software and software within medical devices.
Continuous delivery (CD) is a software engineering approach in which teams produce software in short cycles, ensuring that the software can be reliably released at any time. [ 1 ] [ 2 ] It aims at building, testing, and releasing software with greater speed and frequency.
Associated with the software release life cycle, it was said by Boris Debic of Google Inc. [1] [2] that release engineering is to software engineering as manufacturing is to an industrial process: Release engineering is the difference between manufacturing software in small teams or startups and manufacturing software in an industrial way that ...
Software product management (sometimes referred to as digital product management or just product management depending on the context) is the discipline of building, implementing and managing digital products, taking into account life cycle, user interface and user experience design, use cases, and user audience.
The global IEC 62304 standard on the software life cycle processes of medical device software states it is a "software system that has been developed for the purpose of being incorporated into the medical device being developed or that is intended for use as a medical device in its own right."