Navigating increasingly complex protocols, resource constraints, or the need to scale up faster? We’ve got you covered with flexible service solutions to support you in reaching timelines, achieving data quality, and meeting regulatory compliance.
Wherever you are in your drug, device, or diagnostic development pipeline, Medrio’s expertise and tailored service offerings can help ensure your success. From onboarding and implementation, to building integrations or data management, let Medrio fill the resource gaps in your next clinical trial.
It’s an extraordinary feeling to work with motivated and invested partners like you, our Medrio Team. Because of your confidence, leadership and expertise, I knew we would meet this goal! Thank you from the bottom of our hearts for getting in the trenches with us and making this happen!”
Clinical Project Manager, Global Biotech Specializing in Oncology
Together, we can improve efficiency, simplify communication, shorten study timelines, and deliver better outcomes.
Let Medrio coordinate training, technical project management, and study builds conducted by our Data Sciences team.
We build APIs that share data between Medrio EDC and other software applications and build custom reports.
Our team can manage each step of the eCOA assessment licensing process, including securing author approval.
Allow Medrio to work with translation vendors to convert patient materials into the languages required for the study.
We can coordinate with third-party hardware companies to provide devices to sites and patients.
Customizable services that include eCRF, ePRO, and eConsent design and development, database build, and user acceptance testing (UAT).
One-on-one (or group) meetings with our Data Science Subject Matter Experts (SMEs) to discuss all aspects of your study at the technical level.
Processing study data into a standard structure as part of the submission process to a regulatory authority.
Consultative biostatistician and programming teams dedicated to maximizing your data and delivering high-quality, submission-ready data to regulatory agencies.
Whether you need a true partner or extra hands to navigate a temporary challenge, we can help. Speak with one of our subject matter experts about your business needs and all the ways Medrio can support your goals.
Everything has gone very smoothly with this project. I know it was a small project but the team was really a pleasure to work with. [The Project Manager] kept us on task, [the data scientist] was very knowledgeable and responsive. This study, as a whole, has been a challenge on many fronts so it was really refreshing to have this component go so smoothly. I’m very pleased with the work done and with your responsiveness as well.”
Clinical Project Manager, Global Medical Device
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