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
CDMS / EDC
How to Address Early Obstacles in Phase I
June 10, 2021
It’s no secret that getting new drugs or biological products approved by the FDA is a challenging task. The low rates at which drugs make it all the way through...
Blog
CDMS / EDC•DCT•eCOA / ePRO•eConsent•RTSM
How to Strengthen Trial Retention Through Patient Education
April 30, 2021
According to a 2019 CISCRP study, 85% of the general public are willing to participate in clinical trial research. Yet, recruitment continues to plague the industry as one of the...
Podcast
Patient-Centricity: What Does It Mean and Where to Begin?
This episode will cover dynamic survey design, informed consent, patient diversity, and patient safety as they relate to achieving true patient-centricity in your studies.
Blog
CDMS / EDC•RTSM
How Adaptive Trial-Friendly EDC Benefits Oncology
January 28, 2021
Adaptive clinical trial design in oncology research represents an intersection of two major industry trends. One of these is the current prevalence of cancer clinical trials. Clinical Leader cited a...
Blog
Medrio Inc Names Nicole Latimer as Chief Executive Officer
August 17, 2020
Medrio Inc., the leading provider of eClinical technology to pharmaceutical, biotech, medical device, diagnostics, and animal health markets, announced the appointment of Nicole Latimer to Chief Executive Officer. Nicole will...
Blog
DCT•eConsent
The Future of Informed Consent
August 7, 2020
From eClinical data collection to telehealth to wearables and beyond, the clinical trials industry has seen a mass of technological advances over the past decade. Informed consent is critical to...