Articles, App Notes, Case Studies, & White Papers

  1. 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.

  2. The FDA's Remote Regulatory Assessments: The Future Of Inspections 1/31/2025

    Remote Regulatory Assessments (RRAs) provide distinct advantages over traditional inspections, such as increased efficiency, reduced travel costs, and enhanced global oversight capabilities.

  3. The Impact Of Clinical Trial Payments On Site-Sponsor Relationships 7/18/2023

    The sponsor-site relationship relies on good faith, but late payments sow mistrust. Experts from BMS and CenExel Clinical Research explain how consolidating payment systems benefits both parties.

  4. Do CROs Need To Reinvent Themselves In 2025? 3/21/2025

    Facing economic pressures, regulatory changes, and technological advancements, CROs must redefine their value propositions and discuss the need for reinvention in 2025 to accelerate into the future.

  5. eConsent For Complex Clinical Trials 10/31/2022

    Master protocol design trials require an endless stream of consent forms, adding time, cost, and risk. Learn how a feature-rich eConsent platform can simplify those processes and improve engagement.

  6. The Power Of Predictive Analytics In Clinical Trial Design 10/7/2024

    Discover how predictive analytics address clinical trial challenges by applying statistical and modeling techniques to current and historical data.

  7. Minimizing Hurdles For Patients During The eConsent Process 10/4/2022

    Learn how eConsent digitalizes the trial participant consent process through increasingly simplified models designed to improve comprehension and boost engagement.

  8. Considerations For Implementing The Best eCOAs In Your Trial Design 5/2/2022

    Dive into considerations when deciding on the best COAs to implement as well as best practices when developing your eCOA strategy in this blog.

  9. DTx Company Leverages Real-World Evidence Platform In Registry Study 8/19/2024

    Discover how Castor’s eClinical system enabled a groundbreaking study in behavioral disorder treatment to collect Real-World Evidence (RWE) to support product research and claims.

  10. How A Dedicated Medical Affairs Team Drives Site Engagement 2/15/2024

    See how improvements made to SIP have allowed for quick access to study documents and bulk actions for streamlined document management and enhanced user experience.