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

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Are you ready to ryze??... Transform YOUR trials with our new cloud Clinical MDR & automation suite.


See how CRFs look in Rave, InForm and leading EDCs – as you design in our clinical MDR.

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


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


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

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!

Clinical Metadata Repository (CMDR)

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.


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 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!

What can I do with ryze?

How can our ryze platform help you?

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 FDA and 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.  



instead of 1,484 EDC labor hours


instead of 486 SDTM labor hours


weeks instead of 20 for EDC go-live


weeks instead of 8 to see SDTM data

What can ryze do for me?

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!

Why we're different

With ryze, you can build your study in a fraction of the time it normally takes – in as little as 6 weeks!

We’re the only commercially available off-the-shelf clinical metadata repository. Straight out the box and off you go – we don’t have to custom build it for you from scratch.

Only we integrate 100% with Rave and InForm. So as well as seeing what eCRFs will look like before you build your EDC, you can do complex edit checks and visit structures too. Want to re-import data back into ryze? No problem, you can do that too!

Some companies don’t improve or expand their platform. We do, constantly. We’re always working on new automation stuff, and it’s based on your feedback.

No other platform automatically builds your study in just about any EDC system – 7 to date – saving loads of time. Use your favourite, or even different EDCs for different studies.

Ours is the only fully integrated clinical metadata repository. There’s other clinical metadata repository’s, but they don’t connect with other EDCs or e-clinical systems. We’ve put everything in 1 place, where your content is truly interconnected.

Nobody supports full end-to-end metadata like we do. We cover it all – forms, edit checks, proprietary datasets, mappings and analysis results metadata. And we support every version of CDISC & NCI standards.

Unlike others, you can truly reuse content across multiple EDC systems. Simply drag and drop content from 1 study to another, or one standard to a study – regardless of system. 

Some of the organizations using Formedix



Effortless CDISC compliance

We manage your CDISC compliance. So you don’t have to.


Don’t worry about meeting the latest FDA data standards. ryze supports all versions of CDISC standards. And we keep our platform updated in line with CDISC and NCI standards. That way your study designs and datasets are always regulatory compliant.

As one of the first CDISC members back in 2001, you can rely on our deep rooted knowledge of all things CDISC. We’re members of the CDISC Data Exchange Standards team. As such we’ve been involved in developing many key features in CDISC ODM and Define models. This makes us well placed to give real-world, practical CDISC training. See our CDISC membership certificate for the year 2020-2021. Click below to find out more.  

Got a project in mind?

Tell us what you’re trying to do, and we’ll show you how we can help.