Clinical Operations Roundtable | Boston

Implications for Regulatory Oversight for Outsourced Studies

June 7, 2022 | 3:30 - 7:00 p.m. ET
Location: Veeva Boston, 100 Summer Street, 2nd Floor, Boston, MA

A majority of sponsors outsource clinical trial management in some capacity to CROs, and ICH regulations require that sponsors show proof of oversight. How can you effectively collaborate with your CRO partners to maximize trial outcomes and stay inspection-ready?
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Why Attend

Join your peers at an exclusive roundtable to learn key activities sponsors must do in an outsourced world, including:

  • Reviewing and documenting CRO monitoring events
  • Gaining real-time visibility into TMF status and completeness
  • Simplifying data exchange with CROs
  • Enabling closed-loop issue management
  • Centralizing study training

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Veeva Clinical Operations Roundtable will follow all local guidelines. In accordance with current mandates, masks and proof of vaccination are not required by the City of Boston.