Journal Article: Cheryl Key, Barry Mulchrone and Karen Wai describe an electronic database for tracking RMPs for drugs approved in the European Union and explain why it is crucial for sponsors submitting marketing applications to have a thorough knowledge of safety plans already required for similar products. (Published in the February 2010 issue of The Regulatory Affairs Journal – Pharma)

Award-Winning Poster: This analysis is also presented as a Scientific Poster, which won 1st prize at DIA Europe. "A Review of Additional Risk Minimisation Measures for Products Approved via the European Union (EU) Centralised Procedure"

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