Preparing for the European Medical Device Regulation (EU MDR)
September 27, 2023
Understand how the European MDR (EU MDR) will impact medical device manufacturers and what you can do to prepare.
Medrio Blog
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.
How to Differentiate Your CRO in Today’s Market
May 2, 2023
To stand out in a competitive CRO market, CROs must differentiate themselves by utilizing innovative clinical trial technology and trusted partners like Medrio. This collaboration can lead to efficient builds, reduced timelines, and seamless client experiences, ultimately setting the CRO apart.
5 Ways To Prevent Costly Database Delays
April 17, 2023
Delays in a clinical trial process can have serious downstream consequences, such as missing a go-to-market window or preventing life-changing solutions from reaching the people who need them as soon as possible. Here are five tips to reduce the risk of database delays.
Patient-Centricity Is in Everything We Do: Designing Accessible eClinical Technology
April 11, 2023
Medrio is dedicated to making the clinical trial journey easier by creating thoughtful UX designs that emphasize what’s most important and lead to better participant outcomes. Discover how Medrio provides users with streamlined technology solutions for their clinical trials, as well as tips on improving the participant experience.
ePRO for Early Phase Studies: 3 Ways To Benefit
March 20, 2023
Adopting ePRO in early-phase trials can revolutionize data collection, reduce participant burden and increase the accuracy of results. Not only does this improve patient care, but it also provides commercial advantages to sponsors.