Formedix ryze cloud platform is here!  Learn more 

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

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Fancy a quick look around the ryze platform? Check out our latest demo.

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Easily comply with ever changing CDISC standards & NCI Controlled Terms.

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Hear about UCB's metadata automation journey & how they're achieving standardization.

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Now you can design and build clinical studies FASTER, with LESS effort, and also INCREASE quality!

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!

Clinical Metadata Repository (CMDR)

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!

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Clinical trial automation

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!

What can I do with ryze?

How you’re better off with ryze

Build studies faster - import/export from EDCs

Export your study into your EDC system, straight from ryze. And if you’re using Rave or InForm, you can import studies right back into ryze to make any changes. Even do complex edit checks and visit structures. 

Preview CRF Designs

See what forms will look like in your EDC system at the push of a button. Not happy? Go back, make changes, then preview again until you’re done.

Save time by reusing clinical metadata

Reuse content from one study to another study – even across multiple EDCs. Reuse forms, edit checks, datasets, standards, mappings, annotations… No need to re-type stuff, so you save loads of time.  

Get SDTM datasets before trials start

ryze shows you what your source dataset column headings will be – even before you’ve collected any patient data. So you can do your mappings early on too. By the time you get trial data back, your datasets are all mapped, and it’s just 1 click in ryze to convert to SDTM.

Cherry pick your EDC - don't be tied in

Choose your preferred EDC for your clinical trial building. Even use a different one for each study phase. We integrate with 7 systems, including Rave, InForm and TrialMaster. This gives you huge flexibility – you’re not committed to using a specific EDC system. Mix it up, however you want.

Build your EDC study in 1 click

Happy with your forms? Now it’s 1 click to build you EDC. ryze automates the build process, saving tons of time, so you can start your trials much sooner. 

Effortlessly comply with standards

No worries about meeting regulatory standards. ryze is built on the latest CDISC compliant templates. That means you automatically comply with NCI standards. 

Easily share content & collaborate

Share content and work together from anywhere.  The ryze repository keeps everything in 1 place, allowing teams to work more effectively and efficiently.  

Some of the organizations using our platform

Testimonials

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 and automation tools

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instead of 1,484 EDC labor hours

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instead of 486 SDTM labor hours

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weeks instead of 20 for EDC go-live

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weeks instead of 8 to see SDTM data

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