The $1B Question: How to Never Miss Processing Adverse Events across Your Business (and Always Pass Regulatory Inspections)? – Webcast Replay

We’ve all seen the headlines related to regulatory non-compliance penalties and know the risks, but meeting the challenge of capturing and properly reporting ALL adverse events is a daunting one. Initial receipt of product safety issues is generally from diverse, globally-distributed sources and may be channeled through local safety offices, clinical operations, call centers for medical information or product issues, etc. Initial handling of these items may occur across departments and geographies. Such segregated preprocessing, in an increasing global and often silo’d organization, leads to challenges with reconciliation of received items against those processed in safety systems.


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