A format that is very obviously targeted for the specific use of the busy technologist or manager based in an FDA, WHO or EC regulated pharmaceutical, medical device or bio-technical facility.
Thus enabling these people to quickly raise and issue fully detailed, compliant and professional documents.
It is normally the responsibility of software testers as part of the software development lifecycle.
In simple terms, software verification is: "Assuming we should build X, does our software achieve its goals without any bugs or gaps?
Requirements are usually provided with a unique identifier, such as an ID#, to aid in traceability throughout the validation process.Requirements outlined in the Functional Requirements Specification are usually tested in the Operational Qualification.The Functional Requirements Specification describes what the system must do; how the system does it is described in the Design Specification.Interface requirements Depending on the system being described, different categories of requirements are appropriate.System Owners, Key End-Users, Developers, Engineers, and Quality Assurance should all participate in the requirement gathering process, as appropriate to the system.