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Risk Management Planning and Mandated Post - Authorisation Studies: Risk Management and Late Phase Studies for Real-World Research

Published 19 September 2014 | By PRA Health Sciences

Complex pharmacovigilance legislation in an evolving regulatory landscape has left drug makers searching for current, efficient and more meaningful solutions for their drug safety challenges, especially in the post-marketing arena. Companies are seeking expert advice and customised approaches to effectively collect, manage and analyse real-world evidence for a competitive advantage.

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Risk Management Planning and Mandated Post - Authorisation Studies: Risk Management and Late Phase Studies for Real-World Research