Decentralized Trial Technology Resources

1. The Role Of mHealth Technologies In Clinical Care And Clinical Research 7/12/2022

   Discover how mobile health (or mHealth) solutions provide increased access to care, making it easier for patients to receive care and for healthcare professionals to deliver that care.

2. A Better Approach To eConsent: Flexibility With Enabled Technology 1/11/2023

   Electronic consent, or eConsent, digitalizes the trial participant consent process through increasingly simplified, interactive, educational models designed to improve comprehension and boost engagement.

3. Build Better Studies Faster: 3 Advantages Of Mobile eClinical Platforms 5/7/2024

   Embrace the digital revolution in clinical research with advanced eClinical platforms that expand reach, enhance efficiency, and streamline processes, revolutionizing your trials and work-life balance.

4. How eConsent Is Changing The Informed Consent Process 5/26/2022

   Learn how informed consent — providing a potential participant with enough information about a study to allow for an informed decision about their participation — is a critical step for enrolling patients in clinical trials.

5. EDC For Mid-Study Changes In Medical Device Clinical Trials 6/21/2022

   In this case study, discover how a company was pointed to an electronic data capture (EDC) system that was quick to adapt and easy to scale as the study changed.

6. Direct-From-Patient Data Capture With eCOA 5/2/2022

   Learn how an eCOA tool can provide patients a chance to be heard while giving sponsors quantitative and qualitative data to track the efficacy of a treatment.

7. One Key To Choosing The Best eClinical Technology Vendor 2/29/2024

   Explore why the integration of etechnologies is critical in the modernization and optimization of clinical trials, and how the right partner will ensure studies are more efficient, reliable, and inclusive.

8. 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.

9. Crowdsource UAT: An Opportunity For Future Validation 6/28/2023

   IQVIA, a leading health information technology and clinical research company, has introduced a new validation model for eTMF patterned after approaches used within the larger tech space.

10. Benefits Of Using ePRO In Early Phase Studies 3/24/2023

    Discover how harnessing Patient Reported Outcomes electronically in early-phase trials can boost patient centricity, create more cost-effective operations, and help generate better data faster.