[Webinar Recap] 5 Supply Management Success Factors for Your Early Phase Studies
September 21, 2022
Why it is time to rethink the status quo around randomization and supply management in early phase studies?
Medrio Blog
Four Proven Participant Education Techniques to Improve Electronic Collection of Informed Consent
September 20, 2022
Participant education is a critical part of informed consent and one that is easy to improve by leveraging established patient education best practices. Medrio CEO Nicole Latimer discusses some of the most successful approaches she has seen in her career:
Need Better Clinical Trial Retention? Start with eConsent
September 12, 2022
ICFs can be extremely long and complex. Approaches that prioritize accessibility and promote participant comprehension are key to ensuring a smooth process that supports fully informed consent – eConsent meets those needs while being cost-effective and scalable.
How Are You Labeling Your IP? Protect Your Clinical Trial with Distinct Treatment Numbers
September 6, 2022
Does your CRO or sponsor have a policy around IP numbering in clinical trials? If not, they could be putting your clinical trial at risk.
Winning the Race to FPI with Early Randomization and Trial Supply Management
August 25, 2022
Smart IP Packaging Helps Clinical Trials Avoid Supply Chain Hurdles to Study Startup Ian Davison, Ph.D. Neuroscience, Medrio’s In-house RTSM Subject Matter Expert Packaging decisions may seem benign, but they
Digital Medicine Society Accelerates Recruitment and Results with Medrio’s eConsent
August 23, 2022
The Digital Medicine Society (DiMe), an interdisciplinary professional society for digital medicine, was able to deploy Medrio’s eConsent module in less than two weeks to support its remote study to
Meet Medrio Recap
June 7, 2022
How right-sized, efficient, and cost-effective trial technology solutions can get your devices to market faster. Intro A question we hear a lot from our medical device and MedTech customers is,
Using RTSM to Maximize Supply Chain Efficiency
June 7, 2022
A lot can go wrong in the lifecycle of an investigational product (IP). Medrio’s Randomized and Trial Supply Management system expert, Ian Davison, shares proven strategies that enable teams to
Right-Size Your Technology and Unlock New Efficiencies in Medical Device and Diagnostics Trials
April 29, 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
The The Future of RTSM: Insights and Forecasting with RTSM-Expert, Ian Davison:
April 5, 2022
By all expert accounts, 2022 is the year that we can begin seeing the societal shift from late-stage pandemic to early-stage endemic as the world learns to live with the
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
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!)