Increased regulations and trial complexities—we know all about it. Our solutions and services are designed to help you navigate the ever-changing clinical trial landscape. We invite you to embrace eClinical technology and join us on our journey towards the future of clinical research.
Our user-friendly EDC interface makes it possible for you to build your entire study the way you want it. Its intuitive design means that you don’t need a programmer for every small or mid-study change. But if you find yourself in a jam or need any sort of help, our support team is ready 24/7 to assist you.
Our web-based ePRO solution makes it easier for your patients to report how they are feeling. And get this – it works on any device, anywhere. Whether your patients use it on their home iPad, or your staff access it on a clinical tablet, you can always count on timely and reliable data.
People find consent forms tedious to read and full of complex legal language. As a result, participants are less likely to grasp what is fully expected of them and more likely to drop out later. Our electronic consent tool lets you use plain language and even incorporate video or illustrations to increase understanding and reduce patient drop-out rates.
We know randomization can make or break a study. What if a single solution could help you reduce site overages by 20 – 40% while increasing patient compliance and meeting all of your randomization needs? It would be a game-changer, and we’re here to tell you – we’ve changed the game.
We’ve been innovating eClinical software since 2005 with the intention of simplifying workflows for clinicians and patients. Our Decentralized Clinical Trials Solution is no different. We offer a unified ePRO/eCOA, eConsent, DDC, and RTSM with our EDC. And all of our solutions are designed to meet you where you are and help you reach your goals—in a traditional, hybrid, or fully virtual environment.
Source data validation (SDV) is necessary but time-consuming. Give your sites some valuable time back by empowering them to collect data directly from the source (on or offline) and reduce SDV headaches.
We want you to succeed. Sometimes you need a little extra help to reach your goals. Lean on our experts for everything from study builds, licensing, translations, and more!
You can rest assured that our solutions are fully compliant and secure. We work with external auditors to ensure we’re following all of the necessary protocols, and even a few extra just to be certain. We adhere to the strictest of standards and meet or exceed all global data collection regulations such as ICH/GCP, 21 CFR, GDPR, and HIPAA. You can focus on your trial with complete confidence that your data is compliant with Medrio.
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