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Monday, June 17
 

11:00am PDT

#104: Reporting of Pre-Market and Post-Market Safety Reports to FDA Adverse Event Reporting System (FAERS) Using ICH E2B R3 Standards Room 15AB

3:30pm PDT

#144: Paradigm Shift in Adverse Event Report Management and Sharing: The Case, The Need, and Possible Ways Forward Room 6C #145: Selective Safety Data Collection: As a Tool to Advance Clinical Trial Designs Room 5AB
 
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Ballroom 20 A/ Zone 1
Ballroom 20 BC/ Zone 2
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Ballroom 20 Lobby
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Room 6A,Sails Pavilion
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Sails Pavilion
TBD
USS Midway
  • 00: Plenary
  • 01: ClinSafety-PV
  • 02: ClinTrials -ClinOps
  • 03: Data-Tech
  • 04: MedAffairs-SciComm
  • 05: Patient-Focused Drug Dev
  • 06: TranslationalDelivery Tech-PrecMedicine
  • 07: ProjectManagement-StrategicPlanning
  • 08: RD Quality-Compliance
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  • 10: RegCMC-Product Quality
  • 11: Statistics-Data Science
  • 12: Value-Access
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  • 14: DIAmond
  • 15: Content Hubs
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  • 18: Posters
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