EDC, ePRO, eConsent

  1. Powering Your Research Potential: Exploring Medrio CDMS/EDC 3/14/2024

    In this segment from Clinical Leader's Solutions Expo: EDC Showcase, Medrio CEO Nicole Latimer and Principal Solutions Consultant Jack Cornwall take viewers through an exclusive inside look at their CDMS/EDC solution.

  2. ePROM Implementation: 4 Best Practices For System Functionality 2/13/2024

    Explore four of the 15 system functionality considerations highlighted in an eCOA Consortium article that aim to create a more thorough and standardized approach to ePROM implementation.

  3. Overcoming Real-World Data Capture Challenges In Phase 4 Trials 1/29/2024

    As the demand for real-world insights continues to grow, learn why navigating challenges and leveraging emerging opportunities becomes crucial for advancing clinical research in the real-world setting.

  4. Strategies To Unlock Excellence In DHT Clinical Trials 12/26/2023

    Gain insight into how technology affects patients, critical considerations for selecting the right partners, and potential hurdles in digital health technology trials.

  5. Generating Quality Data To Streamline Trials And Support Approvals 12/8/2023

    Review the highlights from this industry report, which shed light on pathways for optimizing drug development processes, fostering efficiency, and embracing modern technology.

  6. 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.

  7. Medrio eConsent 10/25/2023

    Support the digitization of the participant consent process and begin creating multimedia-enhanced electronic informed consent forms (eICFs) that participants sign electronically, eliminating burdensome and error-prone paper-based processes.

  8. Preparing For The EU MDR 10/5/2023

    Uncover several of the profound impacts the European Medical Device Regulation will have on medical device manufacturers operating within the European Union.

  9. Why eSource Ensures Data Integrity In Medical Device Clinical Trials 7/20/2023

    Learn how eSource data capture offers a more efficient and cost-effective approach to maintaining data integrity.

  10. From Discovery To Pivotal Trials: Enabling Large-Scale Trials For Cancer Detection 6/8/2023

    Gain valuable insights into overcoming challenges associated with large-scale studies and finding the right partner’s role in overcoming technical obstacles.