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See what CRF designs and EDC builds will look like before the trial – even before bid defence stage. Just push a button to preview in Excel, Word, or PDF. Make any changes, and preview again until the client’s happy.

It typically takes around 8 weeks to create SDTM datasets. ryze does it in around 4 weeks – usually less.

No need to become an expert in all the different EDC systems. Build a library in ryze and you can make studies in the top EDCs. Because we integrate with 7 EDCs, your teams don’t need to spend time learning all 7 systems. This saves masses of time and lets you use your resources more effectively.

ryze validates against the relevant rules for each EDC system. So no matter which EDC systems you’re using for clients, your work will always be compliant.

Clients can pick just about any EDC system for their study (we integrate with the leading 7). They could even switch EDCs for different study phases. You can import/export files from Rave and InForm. Then it’s just 1 click for ryze to automatically build the EDC for you.

No worries about meeting regulatory standards. ryze is built on the latest CDISC compliant templates, so you automatically comply with the latest FDA and NCI standards. We support older versions of CDISC standards too, so you’re covered no matter what!

ryze clinical trial software for CROs means you can easily do SDTM mappings and prepare study submissions, like SDTM define.xml for clients. Have everything ready, with no need for SAS or programming knowledge. ryze does it for you.

ryze is the only platform that lets you design CRFs, create SDTM datasets, reuse content, as well as build studies for leading EDCs, and automate SDTM conversions – all in one cloud suite.

ryze is the only Clinical Metadata Repository that lets you design and visualize eCRFs inside the platform. You can see exactly how eCRFs look, and how they work for leading EDCs – without having to build your EDC and go back and forth between platforms to edit and review.

With ryze, you can build your study in a fraction of the time it normally takes – in as little as 6 weeks! Building studies from standardized content not only speeds up design, but also increases quality and consistency across studies and standards.

ryze is the only platform that supports such a breadth of CDISC, 3^rd party, and in-house metadata. You can design CDISC metadata in any version of SDTM, ADaM, SEND, or NCI Controlled Terminology. Plus, you can design edit checks, EDC specific metadata, 3rd party lab transfer specs, mapping metadata, and analysis results metadata to name a few examples.

With ryze, you can transfer metadata between various platforms – such as EDCs – and continually reuse it. There’s no need to redesign, retype, or retest content if you switch EDCs for example. Just move your assets and reuse them. ryze is the only EDC vendor neutral platform that gives this level of reusability across systems.

ryze is the only commercial off-the-shelf solution that’s available for use immediately, and requires very little configuration. ryze can be very quickly tailored to your specific needs, with no long or complex implementation.

ryze is the only solution used by CDISC to design CDASH example CRFs. They create, visualize, edit and approve eCRFs in ryze, then export them in ODM-XML to publish on their CDASH eCRF portal.

You get your first SDTM dataset conversions much faster with ryze – in as little as 4 weeks, or even less! As soon as patient data is live in the EDC, you can see it. So you can act upon trial data far quicker. In fact, our platform was recently used to determine safety and efficacy in several COVID vaccination studies.