Boost profits by being more productive - with less resource

Take on more work – with the same resources – with our clinical trial software for CROs

Build studies faster with fewer resources

More speed – more profit 

Every stage of the clinical study build process is quicker with ryze. Import client’s eCRFs, and use built in templates to speed up dataset design. Our EDC integrations reduce the time it takes to build EDCs. Plus, you can do eCRF designs in Medidata Rave and eCRFs in InForm – directly from ryze! Have the EDC built in around 1/4 of the time. Our SDTM mapping tools automatically create the specifications for you. No double coding. That means you get your SDTM dataset conversion in about 1/2 the time.

Take on more business

Get through client work so much faster with ryze clinical trial software for CROs. Our platform speeds up the end-to-end clinical trial process – from form design to dataset conversion. This frees you up to take on more clients over time.

Less resource – more profit

Increase profit margins by using less resource to get the job done. So many processes are automated in ryze – like EDC build and SDTM dataset creation. Plus you can reuse standards and study content. ryze clinical trial software for CROs makes tasks much easier, and cuts out a lot labor intensive work. Now staff can take on more work, and focus on the profitable stuff, so you can increase margins.

Impress clients & keep them

ryze helps you impress clients by giving better service, and more choice. You get the job done quicker, so can deliver the work faster. And even tough client demands are easy to meet now – like using different EDCs for different study phases. The datasets you give clients will also be accurate, consistent and compliant. All this gives you the opportunity to exceed expectations, and stand out with better customer service.

What can I do with ryze?

How you’re better off with ryze clinical trial software for CROs

Preview CRFs & EDC builds

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.

Get SDTM datasets much faster

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

Save learning time & resources

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.

Effortless validation

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.

Design in many EDCs & build faster

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.

Automatically comply with CDISC

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!

No programming required

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.

Save time by reusing content

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

Organizations using our clinical trial software

moderna logo
UCB logo
vertex logo
University of Alabama logo
cdisc logo
University of Utah logo
argenx logo
idorsia logo
mercator medsystems logo
science37 logo
Catalyst clinical research logo


No programming necessary

Easily map and convert data to submission datasets for clients – with ryze clinical trial software For CRO. Have everything ready, with no need for SAS or other coding skills. ryze automation software does it for you!

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.

You can be hands on or off with clients

ryze clinical trial software For CROs lets you work with clients in different ways. You can manage the whole trial building process from design to submission. Or, just help with specific elements if that’s what the client wants. You can be flexible in other ways too. Let clients only see study designs. Or let them work with you and create new content. See more here about how we make building studies easier for CROs.


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

Got a project in mind?

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


How can Formedix help me save costs?

The Formedix platform automates many of the manual programming jobs usually done by highly skilled, highly paid developers. And, our platform doesn’t require a high level of expertise. That means you can cut down on training expenses and employing highly skilled people.

Can I set user permissions in Formedix?

Yes. In Formedix you can give access to particular users for particular studies. Permissions are set up in such a way that you can grant access only to the study that you want a person to review.

Can I get mid study trial data?

Yes. Our platform lets you see patient data as soon as it’s in your EDC. If your client wants data mid study, then it’s easy to pass it on to them!

Which EDC systems can Formedix integrate with?

Medidata Rave, Oracle InForm, XClinical Marvin, OmniComm TrialMaster, OpenClinica, Parexel DataLabs and Mi-Co Mi-Forms.

If you’re using Rave EDC, you can access existing forms and export them from Rave into Formedix. Make any updates needed and import back into Rave. You can build studies and standards quickly. You can also work on legacy studies that need updated in the same way.

Can I keep track of all changes in Formedix?

Yes. You can instantly see granular difference reports showing changes to standards and studies over time. The platform gives reports showing every change to NCI controlled terminology, CDISC standards, and internal organizational content over time. Formedix can also mock up change management and review cycles for bid defence meetings when you’re trying to win clients.

Can my internal systems integrate with Formedix?

You can use your own API to automate the process of uploading content. You can directly push and pull data between your internal systems and Formedix. No uploading or downloading is needed. You don’t have to login to Formedix. After you’ve done your mappings, you can automatically get your conversion back at the push of a button. This automation saves you lots of time and effort. Find out more about the Formedix API.