EDC/Data Management White Papers & Case Studies
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Emerging Biopharm Rapidly Sets Up Phase 1 Oncology Trial
1/16/2024
Uncover how an emerging biopharmaceutical company was able to expedite the initiation of a Phase 1 oncology trial for a novel treatment targeting relapsed/refractory multiple myeloma.
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Unified, Integrated eClinical Research Solutions
1/16/2024
Facilitate efficient digitalization and optimization of clinical trials that meet the unique needs of small and mid-size biopharma organizations with the Signant SmartSignals Unified Platform.
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An EDC/DDC Solution For Modern Clinical Trials
1/16/2024
Utilized in over 3,000 clinical trials, learn about this comprehensive EDC solution that delivers high-quality data on time and addresses any study team's goals.
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Technology Solutions And Services Tailored For Emerging Biopharma
1/16/2024
Explore how this collection of solutions and services is transforming clinical trials and empowering emerging biopharma organizations to revolutionize medicine.
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How Can Phase 1 Trials Employ eClinical Solutions?
1/8/2024
Uncover how this unified platform is helping sponsors and CROs generate high-quality data, accelerate trials, and rapidly scale to Phase 2 and beyond.
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eClinical Platform Accelerates COVID-19 Treatment Trial By 2 Weeks
1/8/2024
Examine a COVID-19 treatment trial that utilized integrated EDC, eConsent, eCOA, RTSM, and TeleVisit solutions, all within a single platform, to address three critical challenges.
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How MAC Clinical Research Innovates With CDMS/EDC
12/27/2023
Discover how a partnership with one of Europe’s largest contract research organizations exemplifies the crucial role that technology plays in the realm of clinical studies.
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Rave TSDV - Improve CRA Efficiency And Reduce Site Burden
12/20/2023
Source data verification (SDV) is a critical activity within clinical trial monitoring, yet the traditional approach focused on 100% SDV is limited in its ability to quickly identify issues and prevent them from recurring. Rave TSDV (Targeted SDV), unified with Rave EDC, enables CRAs to focus on critical to quality (CtQ) factors identified within risk management activities.
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Managing Risk In Clinical Trials
11/17/2023
Uncover how Risk-Based Quality Management (RBQM) strategies ensure compliance with regulatory guidelines, reduce risks to patient safety, and eliminate inefficient and costly manual processes.
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Zero Disruptions: Migrating 14 Mid-Study Clinical Trials In 16 Months
11/15/2023
Uncover how Imperial College London was able to effectively transfer 14 ongoing studies, encompassing over 1,700 patients and 150,000+ forms, onto a new EDC platform within 16 months.