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Verification and validation are sometimes confused, but they are different activities.
The difference between the two can be summarised as follows: Verification involves checking that the program conforms to its specification.
One of the objectives of this document is to check whether the delivered software system is acceptable.
Structure and documentation is inherent in the way the FDA views testing, but structure does not mean that it must be pre-scripted.
Give your testers assignments on a sheet in a format similar to “Explore _______ With ______ To Discover _______” An example might be: “Explore drug inventory control With a variety of products To Discover if entering the information is intuitive” Or better yet let them have some fun coming up with a bunch of these themselves.
However, flaws and deficiencies in the requirements can sometimes be discovered only when the system implementation is complete.
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Verification will help to determine whether the software is of high quality, but it will not ensure that the system is useful.
The development of software begins once the requirements document is 'ready'.
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