How Medrio Protects Your Clinical Trial Data
November 1, 2023
Explore how to keep your clinical trial data safe, secure, and protected in three key steps.
Medrio Blog
Solutions for Hope: Supporting Participants in Rare Disease Trials
October 26, 2023
Navigating the unique complexities of rare disease research is challenging. Discover key strategies and solutions to support participants and reduce overall burden.
Empowering Oncology Research with the Right Technology Solutions
October 19, 2023
Uncover solutions for oncology trial success: conquer enrollment and retention obstacles, expedite timelines, and navigate global supply chains.
Rare Disease Clinical Trials: Modern Design and Supply Chain
October 10, 2023
Learn unique approaches to study design and supply chain management to better navigate the complex landscape of rare disease clinical trials.
Preparing for the European Medical Device Regulation (EU MDR)
September 29, 2023
Understand how the European MDR (EU MDR) will impact medical device manufacturers and what you can do to prepare.
How Data Is Reshaping the Future of Clinical Trials
September 1, 2023
Data management in clinical research is at an inflection point. Learn what you can do to create more accurate, high-quality clinical trials.
Beginner’s Guide to Electronic Data Capture (EDC) for Clinical Trials
August 22, 2023
The right EDC system can set researchers up for success in building faster, more robust trials. Read more to learn the essential EDC building blocks.
The Moral Obligation: Digital Data Capture for Patient-Centric Trials
August 4, 2023
Digital data capture, such as electronic data capture (EDC), ePRO, and eConsent, create patient centricity and enable accurate data collection.
Why eSource Ensures Data Integrity in Medical Device Clinical Trials
July 14, 2023
Understand the challenges with source data verification and learn how eSource affects clinical trials and improves data integrity.
Importance of Quality Data in Meeting Increasing FDA Regulatory Scrutiny
May 17, 2023
Partnering with a reliable EDC vendor to ensure your clinical trial data meets high standards of accuracy and integrity is essential for passing FDA scrutiny. Risk-based approaches and improved monitoring workflows can help researchers stay ahead of the curve in navigating any potential challenges posed by the FDA, reducing the risk of warnings, rejections or costly additional research.
Want to Boost Retention and Drive Trial Success? You Need Participant Comprehension, Not Consent
May 16, 2023
eConsent is transforming the informed consent process, making it easier for would-be trial participants to understand what’s required of them and providing sponsors with real data on participant comprehension. It’s an important step towards a future of secure, efficient clinical research that serves everyone involved.
Maximizing Data Efficiency: Practical Database Design Tips
May 10, 2023
Effective database design is essential for successful clinical studies, as it improves data quality and accuracy and increases the speed of trial times. This can be done by ensuring the database is user-friendly, utilizing new technologies such as eSource, regularly checking data trends, focusing on SDTM while designing the database, and consulting with sites to proactively address any irregularities. Ultimately, accelerated trial times rely heavily on effective database design.