Patient Data Reporting Applications & Studies

  1. Breaking Free From Process Paralysis In Clinical Trials 1/13/2025

    Explore the implementation of CRIO’s eSource solution by a leading pharmaceutical company to overcome process paralysis in clinical research.

  2. How Syneos Health Tackles Protocol Complexities 1/7/2025

    Explore solutions employed by Syneos Health, a global contract research organization, to optimize Phase IIV clinical trials, particularly under a complex adaptive trial protocol.

  3. How eSource Reduced Benchmark's Protocol Deviations By Almost 40% 1/6/2025

    Explore how a leading vaccine site network selected CRIO to help address the challenges with it's use of paper charts in collecting source data.

  4. Drive Superior Enrollment, Speed, And Quality Using eSource 1/3/2025

    Explore a detailed analysis of 140 research sites involved in a Phase III trial, highlighting significant advancements in trial performance and data quality using CRIO’s eSource platform.

  5. Using eConsent Data To Populate Site And Sponsor Data Systems 10/7/2024

    A top-10 pharmaceutical company was looking to reduce the amount of administrative burden on their clinical trial sites and themselves. See how we accomplished it, using eConsent.

  6. Flexible Integrations To Reduce Risks And Increase Efficiencies 10/4/2024

    Learn how a trial team kept the blind of central lab samples and patient treatment across a Phase III and extension trial, whilst optimizing the supply chain.

  7. Complex Randomization Delivered Successfully 10/4/2024

    Learn about the strategy and successful execution of a complex randomization design that helped LG Chem overcome its clinical trial challenges alongside eClinical randomization experts.

  8. Flatiron Prospective Evidence Generation 9/25/2024

    Explore prospective evidence generation and pragmatic approaches that can help you address staffing challenges and the issue of complexity that is driving up the failure rate of clinical studies.

  9. Overcoming Participant Compliance Challenges In A Medical Device Study 9/9/2024

    Uncover how Catalyst Clinical Research enhanced participant compliance and streamlined scheduling for a TENS device study using the TrialKit platform, with crucial support from CDS.

  10. Fulfilling MDR Requirements For A Groundbreaking Microsurgery Robot 8/19/2024

    Discover the help a company pioneering the field of open surgery received to advance their robotic technology, replacing their former EDC system to improve their clinical research efficiency.