Live demos of ryze Clinical MDR at CDISC US Interchange 2022

Want 1 cloud solution to design CRFs, reuse content, build EDCs and automate SDTM?

Our NEW ryze Clinical MDR & clinical trial automation software gives you everything in 1.


Introducing ryze - the NEW all in one cloud suite to standardize & automate clinical study build

ryze is the only out-of-box clinical MDR and clinical trial automation software suite that lets you design CRFs, create SDTM datasets, build studies for leading EDCs, and automate SDTM conversions – in one cloud platform. ryze has been developed to speed up and streamline the design, build and submission of clinical trials, whilst also improving quality and consistency across studies and standards.

Did we mention it has built-in CDISC compliance! With compliance at its core, ryze features metadata templates with embedded CDISC standards and NCI Controlled Terminology. So you automatically comply with the relevant versions of CDISC. And because ryze is cloud-based there’s zero install. Plus it’s off-the-shelf, so it’s ready to go when you are!


Standardize & reuse metadata

Once metadata content is approved, you can standardize it and reuse it forevermore. It’s there in your clinical metadata repository (CMDR) for everyone to instantly find and manage – like a ‘single source of truth’. Just choose the relevant standards and metadata from your standardized library to quickly and easily build your new study. That means less effort and manual work, and faster trial set up – a major head start if you like! Not to mention improved quality and consistency.


Effortlessly comply with CDISC standards

ryze is built with CDISC compliant metadata templates – including SEND, SDTM, ADaM, Define-XML and NCI standards. Just choose the relevant version of CDISC for your study. Compliance is enforced throughout design and build, right through to submission. Our validation tools highlight any issues and prompt you to fix them as you go.

And ryze stays aligned with new versions and updates to data standards. So you won’t need to manually keep systems or studies updated with changes. That means significant time and cost savings, plus greater quality and consistency in your studies and standards.


Get instant data visibility

ryze significantly cuts lag time, giving you a head start on study build. You can design for market leading EDCs, and see exactly how CRFs look for your EDC – including edit checks, controlled terms and visit structures – as you design in ryze. Because of this, the platform can predict the raw structure of your datasets at form design stage. No need to wait for EDC build. So you get a head start on mappings.  Then you can convert your SDTM datasets early too.

ryze clinical trial automation software gives real-time visibility of trial data as soon as it’s live in the EDC. This enables safety and efficacy decisions to be made immediately, with daily data insights if needed.


What can I do with ryze?

What can ryze clinical trial automation software do for you?

Reuse standardized content

Standardize approved content in your clinical MDR, then reuse it across your standards and studies. There’s no need to start from scratch for new studies, or wade through previous files. Just choose the relevant pre-approved content from previous studies to design your next study.

Design in leading EDCs

Build your study in a choice of leading EDCs, including Rave and InForm. You can even use different EDCs for different study phases. Instantly see how your CRFs look and work as you design them in ryze – then make and view changes directly in the ryze platform. When you’re happy, it’s just one click to build your EDC.

Quickly find and share content

Because your content is stored in one place, it’s quick and easy to find, share and manage metadata. No need to rely on others or waste time searching through files to find what you need.

Easily manage changes and see any impacts

See how proposed changes will impact standards and studies before you make them. Fully control and track all changes – see who made them, and when. ryze gives you full end-to-end traceability, resulting in improved consistency and better decision-making capabilities.

Build datasets faster

Build SDTM datasets quickly using our built in templates. ryze guides you through the process, so you can’t go wrong. You can see exactly how your datasets look as you define them.

Instant SDTM conversions

See your source SDTM datasets before collecting any patient data. That’s a big head start on SDTM dataset design. ryze ‘predicts’ the raw structure of datasets. So you can start your SDTM mappings early too. Then, it’s just one click in ryze to do your SDTM conversion.

Get define.xml in 1 click

Once your datasets and mappings are ready, it’s just 1 click to generate submission-ready define.xml. And our clinical trial automation software lets you can instantly convert Excel or SAS XPT files to define.xml, define.pdf or define.html.

Automatically comply with CDISC

ryze is built on CDISC compliant templates, so you’ll always align with the relevant version of CDISC SDTM, ADaM, and NCI standards. Our validation tools instantly highlight any issues throughout your study, so you can fix as you go and avoid submission delays at the end.

Easily integrate with other systems

Work effortlessly across 3rd party systems. Our APIs let you integrate with other EDCs, e-clinical systems and your internal systems, so you can instantly transfer clinical data into ryze. This saves huge amounts of time and means you can set up automatic processes.

Fancy a quick look around ryze?

Interested in ryze implementation and go-live?

Watch our free webinar “argenx’s Guide to Clinical Metadata Repository Vendor Selection and Go-Live”.


Some of the organizations using ryze clinical trial automation software

moderna logo
UCB logo
vertex logo
University of Alabama logo
cdisc logo
argenx logo
idorsia logo
mercator medsystems logo
science37 logo
aptus clinical logo
datacision logo


Why you get more with ryze

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, 3rd 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.

Clinical metadata repository & clinical trial automation software

Got a project in mind?

Tell us your requirements or what’s giving you grief, and we’ll see if we can help.


Does ryze stay up to date with all versions of CDISC?

ryze supports all version of CDISC standards, including old versions. It’s kept in line with all CDISC and NCI standard updates – so you’re always compliant.

Do I have to use all of the features in ryze?

No. We understand that different organizations have different needs. You can access all of the features in ryze and choose the ones you want to use. For example, some organizations might just want to use the metadata repository to store and manage standards. Some might want to design and build EDC studies. And others might want to use all of the features for their end-to-end studies. It’s entirely up to you.

Can my system integrate with ryze?

Yes. You can log in to your own system and our API automates the upload, conversion and download of clinical data.

What support is available for ryze?

We have a professional services team in place to help and support you. And you get your own dedicated account manager. If there’s something you need doing, it’s no problem. Just let us know what it is.

Can I standardize my content in ryze?

Yes. You can create content from scratch in ryze and standardize it using configurable governance processes that you can set to suit your organization’s needs. You can also import standardized content from your EDC or e-clinical database. By using pre-approved content, you know it’s complete and correct.

Are SDTM conversions automated?

Yes. Once you’ve set up your mappings, it’s just 1 click to convert your compliant SDTM datasets.