Study Start-Up
8 videos · last 6 months shuffled daily, then older videos newest first
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39:11 Planning Around a Respiratory Season That Won’t Hold Still
David LaMarche of ERA Health Research, a site network in Washington state and West Texas, explains why respiratory trials planned on last year's calendar miss the season and how sponsors can activate sites earlier, on a DCN Dx podcast.
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1:47 Stronger Site Partnerships Start with Smarter CDA Alignment
Alison Foster, former VP of development strategy at Fortrea, on how standardising confidential disclosure agreements speeds up the earliest conversations between sponsors and sites.
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56:50 CTSI Open Research Office: Study Start-up: Industry Sponsored Studies
Sevie Kandefer, MS, Clinical Research Associate at UB's Clinical Research Office, on the start-up of industry-sponsored clinical trials.
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34:08 Inventus CEO Steve Sanghera on Clinical Trial Technology
Steve Sanghera, CEO and co-founder of Inventus, discusses its Mobile Device Management solutions for clinical trials, pharma partnerships and the UK government's aim to cut commercial trial set-up times, for pharmaphorum.
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8:27 How the Association of Multisite Research Corporations AMRC Will Improve Clinical Trial Efficiencies
Advarra on multi-site research organisations, and how the Association of Multisite Research Corporations aims to standardise study startup across expanding site networks.
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47:41 AI Protocol Parsing for Study Startup
Cloudbyz shows how its AI reads and translates study protocols into structured data, builds visit plans from schedules of events, and keeps study managers validating the output during study startup.
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1:01:12 Study Start-Up Best Practices From a Site Network
Speakers from the EmVenio Research site network share strategies and case studies for faster study start-up, from protocol feasibility assessments to regulatory submissions and site activation.
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1:02:10 Site Readiness After the Initiation Visit
A OneStudyTeam panel with TASK and Care Access covers gaps left after site initiation visits, managing multiple consent forms and lab manuals, and investigational product preparation at research sites.