Market Expertise

Timing is everything. We understand the pressure to achieve First Person In (FPI) on your schedule, not ours. Our expertly researched solutions put you in control of your processes and any mid-study changes. As a result, you aren’t waiting for us to complete our tasks before you can roll up your sleeves and start yours. More importantly, our role doesn’t end once we enable you to begin collecting data. Our full spectrum service includes study build,  data management, and licensing to ensure your study progresses the way it’s supposed to. We’re here with anything you might need to help you close out the study as soon as your data is complete, accurate, and ready for analysis.

Pandemics and widespread news of rapidly developing vaccines have made transparency and data quality more relevant than ever before. You can trust that our expert staff is extremely knowledgeable of industry regulations. Plus, our integrated platform of solutions makes it easier than ever to monitor and oversee real-time data and ensure its accuracy before you start the analysis phase.  Enhance your reputation by partnering with us on your next study. 

Your studies are typically shorter, smaller, and less complex; you have limited budgets, and you subscribe to a different FDA approval process. Understanding all of these factors, we offer quick and flexible solutions at a reasonable price point. We invite you to become one of the nearly 1,000 device or diagnostic trials we’ve helped support.

We understand that your budgets are often restricted and that your staff typically rely on paper data collection. We also understand your unique challenge of measuring vitals on animals, particularly large herds. Our direct data capture (DDC) solution fits your needs so well it will seem tailor-made. With DDC, you’ll reduce the amount of manual transcription, increase your data quality, and find workflows that are exceptionally well-suited for animal health studies. Our DDC also seamlessly integrates into our EDC, allowing you to have full control over your data, and fewer transcription errors.

Being known for efficient clinical trials increases your chances of partnering with pharmaceutical and diagnostic companies, as well as device manufacturers. Medrio’s enhanced training, excellent customer support (as little or as much as you require), and resources like our Accelegro program are just some of the ways we can establish you as a go-to CRO. We also understand the critical need for oversight and monitoring by your executive staff, which is why our integrated platform of real-time data makes it easy for leadership to run whatever reports they need.