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The relevant authorities must assess the quality of investigational medicinal products based mainly on the parameters "safety of the persons subject to a clinical study", "adequate reproduction of the drug model defined in the clinical trial authorization", and "reliability of documentation". Of these, the safety of the people subject to a clinical study is… (More)
We investigate the usability context that plays a significant role in the design of web sites and in their reception by the users. Usually, the usability context is considered as being hard to be specified exactly. It contains an extensive amount of – possibly even contradicting – knowledge and leads to an adaptation of the user ́s competence. Using a Media… (More)