Resource Library
We’ve compiled a useful collection of resources to learn more about Medrio and various aspects of managing your clinical trial in today’s complex and evolving environment.
Blog
eCOA / ePRO
3 Steps To Improve Site Acceptance of ePRO in Medical Device Trials
March 1, 2023
Medical device organizations aim to reduce development time by 25% in the next five years. The adoption of ePRO can help make this goal a reality.
Webinar
CDMS / EDC
Improve Timelines and Data Quality Across End-to-End Trial Management Processes to Drive Efficiency
The Medrio and Pharmaseal partnership offers a validated data integration solution that simplifies study management. Learn how their integrated EDC and CTMS can eliminate data discrepancies and manual validation in this webinar.
Success Story
CDMS / EDC
Medrio selected again (and again) to support biotech advances in diabetes
Medrio’s electronic data capture (EDC) offers the speed, support, security, and ease of use necessary in the race to uncover biotech breakthroughs to improve the lives of people with diabetes.
Blog
CDMS / EDC•eCOA / ePRO
Nevro Eliminates Two-Thirds of Source Data Verification with Medrio ePRO and EDC
February 23, 2023
Global medical device maker Nevro successfully integrates Medrio EDC and ePRO to transition from paper to digital data collection.
Blog
eConsent
Does Multimedia Have an Impact on Clinical Trial Success?
February 16, 2023
The use of multimedia, including videos, animations, or interactive graphics in clinical trials is growing. Although its impact on the success of clinical trials is not yet fully understood, studies have shown that it can improve participant engagement, comprehension, and retention of study information.
Success Story
CDMS / EDC•DCT•eCOA / ePRO
Innovative Medical Device Company RefleXion Counts on Medrio to Launch First Studies
RefleXion taps Medrio’s service and expertise to help build and launch the first studies for the breakthrough cancer treatment SCINTIX™ biology-guided radiotherapy.