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Standardize and automate your clinical study build with ryze, the NEW cloud-based clinical metadata repository (CMDR) and automation suite. We’ve automated those laborious and expensive manual tasks. Everything from study 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 automatically taken care of for you too. And because ryze is off-the-shelf, you can start straightaway!
Building clinical studies and managing studies is both complex and time consuming. With our 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, there’s no need to start from scratch for every study build. Just choose the content you want to reuse from approved standards and studies in your MDR. Now the pressure’s off! You can build studies in a fraction of the time, and increase quality and consistency at the same time.
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 full EDC with system specific functionality, comply with CDISC, create define files, annotate CRFs, automate SDTM conversions, or validate your study… our new ryze cloud MDR & automation suite makes it quick and painless!
We help pharmaceutical and life sciences teams manage clinical metadata more easily – and get more done! By getting rid of long manual processes, and building in compliance throughout, we make life just that bit easier!