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.
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.
Clinical trials are complex and time-consuming, but using your EDC shouldn’t be. Many systems are riddled with inefficiencies that result in lengthy, expensive study builds, cumbersome mid-study changes, and delayed access to crucial study data. 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 …
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 understand your unique challenges and how to solve them.
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 eSuite is flexible and intuitive so you can execute on bids efficiently while increasing build speed, data quality, and sponsor trust.
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.
The nature of managing clinical research has evolved greatly since the initial clinical trial management systems (CTMS) and other early eClinical technologies were introduced. As the traditional trial paradigm has shifted, new technologies have been introduced and existing ones have evolved to keep up with the industry. As trial operators look to the future of clinical research, it’s imperative that …
Now, more than ever, sponsors and CROs need to prioritize including patient engagement in their study builds from the ground-up. This involves defining processes to remove barriers for access, increasing awareness and education for clinical trials, and creating effective exchanges between patients and their clinicians. Complete the form below to get instant access.
When your trials rely on an investigational product (IP), your study timeline, budget, and overall success are closely tied to having the right product available at the right time and site. Once randomization is added in, sponsors can struggle to maintain an increasingly complex supply chain. Achieve operational efficiency with RTSM. Complete the form to get instant access.