Why formedix? Speed. Compliance. And ROI.
Want to get your clinical trials designed, built & submitted much faster?
Now you can, with our off-the-shelf clinical metadata repository (MDR) and clinical trial automation software. We’ve taken away those time-consuming and expensive manual tasks, from study set up to submission.
Our clinical metadata repository provides a central home for your organizational standards. Here you can manage, update, approve and resuse your standards. All whilst keeping on track with CDISC standards, and complying with regulatory requirements. You can even share and reuse content across different EDC and e-clinical systems.
And if you need help automating study design and build, we can do that too. Our clinical trial automation tools use the content in your metadata repository to help build your studies much faster. Whether you want to annotate CRFs, build EDCs, make SDTM datasets, create define files, or validate your study… Formedix helps you do it in a fraction of the time. Quick and painless.