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.
Webinar
eConsent
Meet Medrio Episode 1, Part 1: Patient Engagement Solutions
It’s no secret that patient recruitment and retention is one of the most significant challenges in clinical studies. With 35% of patients who dropped out of trials citing the consent form as confusing, you have an opportunity to ensure that your study’s consent process is simplified and designed for patient comprehension.
Blog
DCT•eCOA / ePRO•eConsent
Think Paper is the Safe Choice for Your Studies? Think Again.
March 24, 2022
It’s 2022—the world is embracing digitalization on a mass scale, yet 76% of healthcare organizations admit to printing their consent forms on paper. Why does the clinical trials industry continue to think that...
Blog
Medrio Proudly Joins Association for Clinical Data Management (ACDM)
March 13, 2022
San Francisco, CA, March 13, 2022 – Medrio announced today that they have joined The Association for Clinical Data Management (ACDM). Medrio is excited to become part of ACDM and engage globally...
Blog
It’s Time for Healthcare to #BreakTheBias
March 8, 2022
It’s 2022—over one hundred years have passed since the women’s suffrage movement; women make up more than half of the college-educated workforce; and the U.S. has our first female Vice President. But, many of us continue to ask, “Is that enough?” (Hint: the answer is a resounding NO!)
Blog
CDMS / EDC•CTMS
Medrio, Inc. and PHARMASEAL Unite to Offer Streamlined End-to-End Data Collection and Management for Clinical Studies
September 28, 2021
Medrio, Inc., a leading provider of decentralized and eClinical technology to pharmaceutical, biotech, medical device, diagnostics, and animal health markets and PHARMASEAL International Ltd., a provider of clinical trial management...
Blog
eSource
How eSource Optimizes The Clinical Site Experience
September 7, 2021
Trial sites are a cornerstone of clinical research but are often overloaded with a myriad of complex, manual, and time-sensitive tasks. How can sites be expected to create a positive...