Medrio eConsent: Put Patients First and Reduce Drop-Out
With 85% of studies failing to retain enough patients, 30% of patients dropping out of studies, and 8% of those patients dropping out due to failure to understand study requirements,
With 85% of studies failing to retain enough patients, 30% of patients dropping out of studies, and 8% of those patients dropping out due to failure to understand study requirements,
The process for bringing medical devices to market is increasingly complex. From regulatory challenges to the growing number of new data endpoints—device researchers, sponsors, and CROs need nimble tools that
Clinical trials are complex and time-consuming, but using your EDC shouldn’t be. You need a reliable, central hub that maximizes your efficiencies and allows you to reach your goals sooner—all while tightening up your costs and giving you full control over your clinical trial research.
Phase I clinical trials represent a major milestone in a new medical product’s journey from lab to market. The insights gathered from testing a product on humans is key to
Your ticket to faster insights from patient-reported data, more control over timelines, and improved patient engagement.
The benefits to your patients and your team are plentiful. Removing the patient burden of always coming into the clinic increases recruitment, compliance, and patient engagement.
We frequently engage with external auditors to ensure we’ve followed all of the necessary software and procedural controls. When joining Medrio, you can be confident that your data is secure
Do you have trouble recruiting and retaining patients for your trials? And when an unexpected change happens mid-study, do you lose valuable time waiting for someone to get back to
Randomization & Trial Supply Management brings a positive impact to your study. Just optimize RTSM once and continue using it in future clinical trials.
What if you could receive high-touch, white-glove eClinical support at no additional cost to you? With Medrio, now you can.
It’s important that we give you a good foundation to be successful with your eClinical suite. Our Professional Services team is comprised of knowledgeable product experts and data scientists who
Boutique CROs know that no two studies are the same. You aim to deliver high-quality, white-glove service to your sponsors and need an adaptive eClinical suite behind you. Medrio’s integrated
Clinical trial operations management is no easy feat. From competing demands, regulatory pressures, and budget constraints—you can’t afford to rely on unreliable data.
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