ArisGlobal

On-Demand Webinar: Global Regulatory Update


After a relatively quiet period, 2015 and 2016 will see a raft of regulatory changes that impact both pharmacovigilance and regulatory departments – sometimes in related cross-functional areas. In this webcast Mark Loudon will provide an update covering recent and upcoming changes, with an emphasis on how these areas will impact safety and regulatory, with practical discussions of ways to achieve efficient, cross-functional compliance. Areas of discussion will include: mandatory electronic reporting, the shift from E2B(R2) to E2B(R3), risk-information flows between safety and regulatory.

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