Articles, App Notes, Case Studies, & White Papers

1. Comparative Effectiveness Of eConsent: Systematic Review 4/17/2024

   This blog post examines eConsent vs. ICF on comprehension, acceptability, enrollment, retention, consent time, and site workload.

2. 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.

3. Accelerated Approval As The New "Norm" In Gene Therapy For Rare Diseases 5/13/2025

   Gene therapy has revolutionized treatment prospects for rare genetic disorders by enabling corrective or replacement strategies at the molecular level.

4. How To Improve Patient Outcomes Using eSource Software In Clinical Trials 8/11/2025

   As the demand for patient-centric clinical trials grows, eSource platforms will play an increasingly vital role in facilitating efficient, compliant, and innovative research methodologies.

5. Automated Trial Monitoring Workflows Make Small Teams More Efficient 4/13/2023

   A pharmaceutical therapy developer was looking to automate reports, confirmation letters, and follow-up letters. See what happened when they adopted a cloud-based solution for end-to-end trial management.

6. Configurability And Customization: Key Features In An eTMF Solution 3/2/2023

   Discover how a configurable and customizable eTMF can lend itself to better information control during a clinical trial while boosting security and regulatory compliance efforts.

7. Making The Lives Of Patients And Research Sites Easier 5/14/2025

   Most clinical trials overlook one crucial factor: giving sites and patients a voice in how studies are run. That’s starting to change—and the impact is significant.

8. Blinded Randomization And Trial Supply Management Gets Support 11/17/2023

   Uncover how this global specialty pharmaceutical company was able to ensure the confidentiality of its blinded study data while receiving flexible and scalable unblinded support.

9. Elevating Rater Training For More Reliable Study Outcomes 2/21/2025

   Well-trained raters are key to generating high-quality, consistent clinical trial data. Explore a program offering customized training tailored to the experience levels of raters.

10. FDA Releases Updated Draft Guidance On Decentralized Clinical Trials 6/12/2023

    Take a closer look at the FDA's draft guidance on designing and implementing DCTs, notably remote trial visits, the use of digital health technologies, institutional review board oversight, and more.