How Standardizing Data Collection Enables Scalability in Clinical Trials
April 25, 2024
Learn from Roche Diagnostics about how to standardize electronic data capture for higher quality data and scalability.
Medrio Blog
2024 MedTech Regulatory Updates: 4 Areas of Interest
March 21, 2024
Learn key areas of focus for MedTech regulations in 2024, as trials become more complex and new technologies continue to emerge.
Rare Disease Research: Finding Participants and Driving Progress
February 26, 2024
Explore recruitment and engagement strategies in the dynamic landscape of rare disease research, where participants and advocates drive progress.
Supporting Early Phase Oncology Research with the Right Data Management System
February 20, 2024
Innovating in early phase oncology trials requires the right clinical data management system. Find out what to look for!
ePROM Implementation: 4 Best Practices for System Functionality
February 13, 2024
Understand best practices for implementing electronic patient-reported outcome measures (ePROM).
Overcoming Real-World Data Capture Challenges in Phase IV Trials
January 22, 2024
Learn how to leverage real world data (RWD) and real world evidence (RWE) for impactful phase IV clinical trials.
Mastering eConsent: 3 Proven Implementation and Adoption Best Practices
January 5, 2024
Unlock the benefits of electronic consent (eConsent) with our expert insights on adoption and implementation.
Strategies to Unlock Excellence in Digital Health Technology Clinical Trials
December 19, 2023
Discover expert insights for digital health technology clinical trials, including regulatory strategies, endpoint selection, and trial design tips.
Clinical Research 2023: Highlights and Headlines
December 15, 2023
Dive into the highs and lows of 2023 in clinical research! Explore groundbreaking studies, regulatory milestones, and the latest in digital therapeutics in this year’s top news recap.
Generating Quality Data to Streamline Trials and Support Approvals
December 1, 2023
Uncover clinical trial design and execution solutions for collecting high-quality data for approvals.
Re-Consent in Clinical Trials: Streamlining with eConsent
November 20, 2023
Learn about re-consent challenges, regulatory insights, and the role of eConsent in streamlining informed consent processes.
Is Your Clinical Supply Chain Fully Optimized?
November 15, 2023
Unlock key clinical trial supply chain optimization strategies to ensure efficient logistics, reduce waste, and streamline operations.