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Medicinal product evaluation is one of the most important tasks undertaken by government health departments and their regulatory authorities, in every country in the world. The automation and adequate software support are critical tasks that can improve the efficiency and interoperation of regulatory systems across the world. In this paper we propose a(More)
The complex procedure of processing the marketing authorisation of medicinal product licences is a challenging task for government health authorities and the pharmaceutical industry across the world. Regulatory requirements have diverged significantly, and each country has its own regulations and procedures for marketing authorisations. The automation of(More)
Quality indicators for performance management of the UK National Health Service have been introduced for general practitioners (GPs) in order to monitor if they are meeting their performance targets. Such requirements impose significant load to GPs' everyday operations and any type of software solution that stores relevant information and addresses(More)
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