Abstract
During the development of a number of drug information systems, the SWEDIS Development Center has gained a lot of experience in the strategy of software development within the drug regulation environment. Software must be validated to ensure that it does what it is expected to do and will continue to do so. With the help of some simple strategies, software used in clinical research can be validated. The software will also continue to run in new environments if it is developed using independent interfaces to the environment.
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