Search results
Results from the WOW.Com Content Network
Verification is intended to check that a product, service, or system meets a set of design specifications. [6] [7] In the development phase, verification procedures involve performing special tests to model or simulate a portion, or the entirety, of a product, service, or system, then performing a review or analysis of the modeling results.
Software validation checks that the software product satisfies or fits the intended use (high-level checking), i.e., the software meets the user requirements, not as specification artifacts or as needs of those who will operate the software only; but, as the needs of all the stakeholders (such as users, operators, administrators, managers ...
The easiest way is to say that verification is always against the requirements (technical terms) and validation is always against the real world or the user's needs. The aerospace standard RTCA DO-178B states that requirements are validated—confirmed to be true—and the end product is verified to ensure it satisfies those requirements.
ISO 13485 Medical devices -- Quality management systems -- Requirements for regulatory purposes is a voluntary standard, [1] published by International Organization for Standardization (ISO) for the first time in 1996, and contains a comprehensive quality management system for the design and manufacture of medical devices.
Verification and validation of computer simulation models is conducted during the development of a simulation model with the ultimate goal of producing an accurate and credible model. [ 1 ] [ 2 ] "Simulation models are increasingly being used to solve problems and to aid in decision-making.
Another approach is deductive verification. [5] [6] It consists of generating from the system and its specifications (and possibly other annotations) a collection of mathematical proof obligations, the truth of which imply conformance of the system to its specification, and discharging these obligations using either proof assistants (interactive theorem provers) (such as HOL, ACL2, Isabelle ...
Standards for validation and verification of medical laboratories are outlined in the international standard ISO 15189, in addition to national and regional regulations. [1] As per United States federal regulations, the following analytical tests need to be done by a medical laboratory that introduces a new testing device:
These specified procedures and outlined requirements lead to the idea of Verification and Validation and software testing. It is distinct from software quality assurance which encompasses processes and standards for ongoing maintenance of high quality of products, e.g. software deliverables, documentation and processes - avoiding defects ...