Articles, App Notes, Case Studies, & White Papers

  1. Paving The Way For Virtual Trials In Neurology: A Fully Remote ALS Study 5/23/2023

    The COVID-19 pandemic has completely changed the way we think about clinical research and care. Clinical trials, a vital component of the drug development process, were heavily disrupted because patients, often with weakened immune systems, could not visit hospitals and research sites.

  2. Can Your Clinical Trial Design Handle Mid-Study Changes? 9/25/2023

    Mid-study changes are frequently inevitable, but it’s possible to reduce the downtime they create with strategic planning and technology. See how to plan for mid-study changes that mitigate downtime.

  3. Wearable Data Is Only Useful If It's There: Helping You Collect Your Study Data 9/15/2025

    New, proactive alerts on this digital health platform ensure complete and high-quality data collection from wearable devices in clinical trials.

  4. Maximizing Site Performance: The Hidden Benefits Of Unified eConsent And EDC 12/6/2024

    Disconnected systems for eConsent and EDC create inefficiencies that burden clinical trial teams, but modern integrated platform solutions are streamlining operations.

  5. Strong eCOA Provider And Linguistic Validation Expert Partner For Success 7/26/2022

    Explore the creation and implementation of the electronic versions of COAs (eCOAs) on a high priority study with a new client.

  6. Endpoint Reliability And eCOA Solutions Facilitate CNS Trial Success 8/15/2023

    A Japan-based pharmaceutical development company utilized Signant's eCOA solutions and knowledge to ensure the reliability of endpoints in their Phase 3 and extended-duration CNS trials.

  7. Harnessing The Power Of eCOA Technology 11/29/2023

    Get an overview of this COA-focused panel at the C3 Summit in London where industry experts and leaders discussed challenges, opportunities, and strategies in clinical trial diversity, centricity, and outcome assessments.

  8. Discover The Value Your eTMF Should Deliver 3/7/2022

    A well-prepared Trial Master File (TMF) is critical to the success of any clinical trial. Because the TMF tells the whole story of a study – including every data point collected and decision made – managing it throughout the course of the trial is challenging.

  9. Preparing Studies With eConsent For IRB Approval 6/7/2023

    Understand how eConsent can benefit trials and align with IRB ethical commitments, how to prepare your IRB submission for approval, and the future impact of large language models.

  10. Re-Consent In Clinical Trials: Streamlining With eConsent 11/29/2023

    Delve into a variety of triggers for initiating re-consent, perspectives of regulators and IRBs regarding the re-consent process, and the role of digital processes in preventing issues related to re-consent.