EDC/Data Management White Papers & Case Studies

31. Veeva Clinical Database Features Brief 6/21/2024

    See how the Veeva Clinical Database (CDB) aggregates, cleans, and transforms clinical data from multiple sources to ensure comprehensive and accurate data management for your clinical trials.

32. Bring Your EDC Study In-House 6/17/2024

    The EDC module with Signant SmartSignals^® Unified Platform, trusted in over 3,000 trials, allows in-house teams to design studies easily with minimal training and no coding skills needed.

33. Our Unified Platform Serves As eSource For COVID Treatment Trial 6/17/2024

    Signant Biotech optimized technology for an emerging biopharmaceutical's Phase 2 COVID treatment trial in critically ill patients, minimizing paper data risks and streamlining consent and data management across multiple sites and solutions.

34. How Optina Diagnostics Used EDC In Earlier Disease Detection 5/15/2024

    Understand how Optina Diagnostics streamlined operations and achieved significant milestones by leveraging Castor's tools in its effort to revolutionize the diagnostic process for Alzheimer’s.

35. The Path To Proof, Reimagined 5/15/2024

    By combining technology with clinical and operational expertise, Signant Health prioritizes the clinical research stakeholder experience, making it more intuitive, while ensuring the data journey is direct.

36. One Home for Sites™ Partnership Program Guide 4/7/2024

    Learn how your organization can become part of One Home for Sites, the only platform that’s bringing the industry together to help sites survive and thrive, along with their patients.

37. Unified Platform Solutions For Phase I Clinical Trials 3/19/2024

    Phase I clinical trials need technological solutions that support rapid implementation and end-to-end processes. Signant’s unified eClinical platform provides the perfect partner for Phase I research.

38. Driving Customer Profitability With Enterprise Platform, Pricing 2/29/2024

    Explore how the solutions and approaches offered by CDS can help different research stakeholders conduct more cost-efficient clinical trials in the industry's pharmaceutical, biotech, and device sectors.

39. From Paper To Digital Study Management In Large Patient Registries 2/13/2024

    Uncover how this sponsor was able to independently design and oversee its clinical study, minimizing external assistance, and easing the workload for their sites through mobile app accessibility.

40. Achieving Self Sufficiency In Data Collection For Optinose 2/12/2024

    Uncover how this specialty pharmaceutical company was able to gain control over its EDC environment by adopting a solution their team could use in-house.