Trial Efficiency and Collaboration Key Topics at 2020 Veeva R&D and Quality Summit | Veeva
Summary
This view was echoed by Marc Nephtali, Jessica Skrine, and Garrick Myers from Vertex Pharmaceuticals, who modernized its operating model by unifying clinical systems throughout the enterprise. Jess Robinson from GSK discussed the importance of aligning people, processes, and technology to achieve a unified clinical environment and speed study execution. Leila Ponce, clinical trial manager from Seagen, explained how metrics, dashboards, and reports built within Veeva Vault eTMF are used to maintain an ongoing culture of inspection-readiness, and subsequently, helped the TMF team prepare for, and pass, an inspection. Leveraging Vault eTMF to streamline TMF processes and improve inspection readiness was a priority for JC Sheridan and Heather Frankhouser from Janssen. Jeff Wiley, head of global clinical project delivery at Covance, broached the difficulties in monitoring and source data verification (SDV) activities once COVID-19 hit.
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