Featured Articles
-
Digital Medicine Society Accelerates Recruitment and Results With eConsent
9/26/2022
Find out how the Digital Medicine Society (DiMe), an interdisciplinary professional society for digital medicine, was able to deploy an eConsent module in less than two weeks to support its remote study to assess nocturnal scratching as an endpoint for patients.
-
Better eConsent Through Education Best Practices
9/23/2022
eConsent can have a positive impact on participant retention, but learn why that is only part of the challenge of meeting participant needs in a clinical trial.
-
It’s Time For Healthcare To #BreakTheBias
9/13/2022
In anticipation of International Women’s Day on March 8th, Medrio’s female leadership were asked to reflect on the state of female equity in the healthcare industry. These are their experiences.
-
Think Paper Is The Safe Choice For Your Studies? Think Again.
9/13/2022
Why does the clinical trials industry continue to think that paper forms are sufficiently safe and equipped to handle their patients’ most sensitive data? Find out the answer in this blog.
-
TargetCancer Foundation Successfully Engages And Empowers Rare Cancer Patients
9/13/2022
Delve into how the TargetCancer Foundation implemented a remote consent function in their TCF-001 TRACK study with an objective to determine if rare tumors can benefit from matched molecular therapy.
-
Right-Size Your Technology And Unlock New Efficiencies In Medical Device And Diagnostics Trials
9/13/2022
With the constant pressures to do more with less, it can be overwhelming for medical device and diagnostics (MDD) researchers to plan out clinical trials while supporting the vast array of technology and services.
-
How Are You Labeling Your IP? Protect Your Clinical Trial With Distinct Treatment Numbers
9/8/2022
Explore why engaging randomization and trial supply management (RTSM) services early in study startup can help protect clinical trials and expose substantial efficiencies, effectively baking in practices that help streamline supply chains.
-
Winning The Race To FPI With Early Randomization And Trial Supply Management
9/8/2022
Learn why the ability to get investigational products to sites, and appropriately store them, is not a given – and this oversight can have serious consequences.
-
How Unified Trial Management Future-Proofs Clinical Trials
2/10/2022
This paper will explore the ways that unifying the eClinical stack can help future-proof your clinical trials.
-
Achieving 97% Patient Compliance, Increased Patient Engagement
9/23/2021
In a proof-of-concept for a decentralized hybrid study, explore how Electronic Patient-Reported Outcomes (ePRO) technology was used to assess the results of varying digital therapies and the feasibility of conducting a largely virtual clinical study in a fibromyalgia population.