Efficient Pharmacovigilance Process Based on Document Management

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Published 28 September 2011 | By Infotehna Group

Each company has to establish a pharmacovigilance system, with the primary aim of ensuring timely gathering, analyzing and submission of safety concerns. This documentation is the primary target for any pharmacovigilance audit and thus has to be maintained in a way similar to GMP documentation. INFOTEHNA solution provides profiles for all of the necessary documents, with predetermined templates, lifecycles, workflows and roles.

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