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Standardize and automate your clinical study build with Formedix ryze, the NEW cloud-based clinical metadata repository (CMDR) and automation suite. We’ve automated those laborious and expensive manual tasks – throughout set up to submission. And given you the tools to standardize clinical trial design and build. So now you can build studies in as little as 6 weeks! CDISC compliance is taken care of too, with our metadata templates and validation tools. And because ryze is off-the-shelf, you can start straightaway!
Building clinical studies is complex and time consuming. With our ryze Clinical Metadata Repository (CMDR), all your content is in one place. So you can easily find, manage, share – and importantly reuse content – even across different EDC and e-clinical systems.
Once you’ve standardized your metadata, you don’t need to start from scratch for every study build. Just choose the content you want to reuse from approved studies and standards in your MDR. So you can build studies in a fraction of the time, and increase quality and consistency too!
Gets studies designed and built faster with ryze clinical trial automation capabilities. Whether you want to design and visualize CRFs for leading EDCs, build your EDC with system specific functionality, comply with CDISC, create define files, annotate CRFs, automate SDTM conversions, or validate your study… our new ryze cloud-based automation suite makes it possible!