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Operationalizing the Serious Adverse Event (SAE) Process at Clinical Research Sites

by SOCRA | Jul 19, 2021 | Clinical Research, Monitoring, Project Management, Protocols, quality management, Trial Management

Tracy Popp, MBAPreviously: Director, Research Financial Operations Norton Healthcare, Inc.Currently: Senior Director of Clinical Research, Tampa General Hospital Abstract: It is important for clinical research sites to operationalize the serious adverse event (SAE)...

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Promoting excellence in clinical research professionals through education, CCRP® certification, and community, leading to ethical, high-quality research, protection of participants, and global health improvement since 1991.