Featured Articles

  1. Automated Study Calendaring For Clinical Trials 8/18/2024

    Uncover this groundbreaking automated study calendaring system, designed to revolutionize clinical trials by streamlining scheduling, enhancing user engagement, and ensuring timely data collection.

  2. Efficiency & Quality: The Impact Of CDASH eCRFS On Clinical Trials 7/16/2024

    Discover how CDASH eCRFs are transforming clinical trials, enhancing efficiency and quality through validated standards and streamlined data collection, benefiting both study designers and participants.

  3. Four Ways To Strengthen Patient Engagement In Clinical Trials 6/19/2024

    Interest in clinical trials is rising, with more people willing to participate. Here are four ways to strengthen patient engagement and enhance their experience in clinical research.

  4. One Easy Way To Reduce Data Errors And CRC Burnout 6/19/2024

    See how the implementation of cross-form logic can minimize data errors and alleviate burnout for clinical research coordinators handling complex trial data entry.

  5. The Stakeholder Benefits Of EHR eSource In Clinical Trials 5/15/2024

    Discover the transformative power of EHR eSource integration through the eyes of a clinical research coordinator and project director in an adaptive platform trial.

  6. Eight Ways Medical Device Clinical Trials Differ From Drug Trials 5/15/2024

    Delve into the nuanced disparities between medical device and drug clinical trials with eight critical differentiators shaping regulatory pathways and patient safety.

  7. How Different Are Oncology Clinical Trials? 3/19/2024

    Oncology clinical trials pose unique challenges. Dive into five key reasons behind the intricacies of oncology trials, from recruitment hurdles to data volume and efficacy endpoints.

  8. The Workhorse Of Today's Clinical Trials 3/19/2024

    Unlock the power of decentralized clinical trials with an electronic data capture platform (EDC). Discover how stakeholders benefit and what to consider when choosing the right EDC system.

  9. Let's Get SMART On Adverse Events 1/17/2024

    One of the biggest risks for medical products and companies is the failure to report adverse events. But what leads to underreporting? Here are five core reasons behind most adverse event underreporting.

  10. Everyone's Talking About: Our Most Read Blogs Of 2023 1/17/2024

    Discover the latest insights and trends shaping the landscape of clinical trials, like SMART on FHIR, patient-centered trials, eSource, and eConsent, with OpenClinica's most popular blogs of 2023.