Want to get your clinical trials designed, built & submitted, faster? 

Now you can, with our off-the-shelf clinical metadata repository and study automation platform. We’ve automated those time-consuming and expensive manual tasks, from study set up to submission. 

Our clinical metadata repository (MDR) provides a central home for your organizational standards. Here you can manage and update your standards – whilst keeping on track with CDISC standards, and complying with regulatory requirements. You can even share content across different EDC and e-clinical systems. 

And if you need help with study automation, we can do that too. Our study automation tools use the content in your metadata repository to help design and build your studies much faster. Whether you want to build EDCs, create define files, annotate CRFs, convert datasets, or validate your study… Formedix makes it quick and painless.

Clinical Trials

Health Care

Health Data

Life Sciences

Formedix

Formedix's headquarters in Burlington, MA, United States

Mark Wheeldon

Katrina Merry

Greg Blincow

Quality Assurance and Testing Team

Software Development Team

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Formedix

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