Articles, App Notes, Case Studies, & White Papers

  1. eReg Benefits For Clinical Research: Use Cases For All Types Of Sites 5/1/2023

    Unearth the different kinds of eRegulatory use cases for diverse clinical site types and other eRegulatory capabilities designed to serve all sites.

  2. Open API Provides Better Access, Freedom To Build And Manage Studies 2/29/2024

    Discover how the integration of all manner of data platforms ranging from central labs to CTMS and beyond can help to overcome interoperability challenges in clinical research.

  3. Case Study: How Real-World Data Optimized An Oncology Clinical Trial Protocol 7/23/2024

    Many challenges in running clinical trials are difficult to prepare for, but some, such as trial enrollment and study operational execution, can be proactively addressed thanks to advances in high-quality RWD.

  4. How Site eSource Completes And Extends The EHR To EDC Initiative 7/7/2025

    This study evaluates to what degree an eSource-to-EDC data transfer initiative succeeds through two key dimensions: "Mappability" and "Prevalence".

  5. How Flatiron Supported The Beat AML® Master Clinical Trial 9/16/2024

    Find out how the Leukemia and Lymphoma Society's partnership with Flatiron Health helped improve the Beat AML® Master Clinical Trial's data management and accelerate trial timelines.

  6. Achieving Faster, Simpler Validation Through Crowdsource UAT 6/28/2023

    An approach most often seen in the larger tech space, crowdsource UAT can offer several potential advantages for the clinical trial industry and eTMF validation.

  7. 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.

  8. Break The Contracting Bottleneck To Speed Site Activation 10/23/2024

    With the appropriate training data, AI has the capability to automate information gathering, document creation, and workflow management.

  9. A Data-Driven Approach To Clinical Trial Site Selection 3/24/2025

    By incorporating data-driven site selection and verification, sponsors can optimize resource allocation, enhance protocol compliance, and improve overall trial integrity.

  10. 3 Benefits Of Centralizing Global Content For eCOA Migration 9/23/2022

    Learn why now, more than ever, sponsors aim to empower the global patient voice through patient-centric technologies—including providing wearable technologies and using electronic clinical outcome assessments (eCOAs) to collect patient data.