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Boost margins with our clinical trial automation software

That’s what you can expect when you start using our study automation platform.

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Less labor, faster study build, with clinical metadata management

CRF designs. Making annotations. Building studies in different EDCs. SDTM mapping. SDTM conversion… And all while trying to satisfy client demands. ryze helps you do all these tricky and time consuming things – FAST. And with fewer resources too! You can download our flyer for more information.

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. 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. All this makes tasks much easier, and cuts out a lot labor intensive work. Now staff are freed up to take on more work, and 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?

What can ryze do for me?

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

CROs 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.

Clinical metadata repository & clinical trial automation software

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API
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CRF design & EDC design
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SDTM Datasets, SDTM Mapping & SDTM Automation
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Visual define.xml editor
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Annotated CRFs
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Validation
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No programming necessary

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

Some of the organizations using Formedix

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Testimonials

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! 

No other clinical trial automation software saves you time by building your study in almost any EDC system. That’s 7 to date. Use your favourite, or even different EDCs for different studies.

Only we integrate 100% with Rave and InForm. So as well as seeing what something will look like before you build it, you can do edit checks and preview eCRFs too.

Unlike others, we keep pace with version changes in CDISC standards, so you’ll always be compliant.

Unlike others, you can truly reuse content and save time. No need to retype spreadsheet contents for example. Simply reuse standards and study content between studies – even across multiple EDC systems.

Ours is the only fully integrated clinical metadata repository out there. There’s other clinical metadata repository’s, but they’re like disconnected libraries. We’ve put everything in 1 place, where your content is truly interconnected.

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.

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

Work flexibly with clients

ryze clinical trial automation software lets you work with clients in different ways. You can manage the whole process from form design to submission. Or just help with specific tasks if that’s what the client wants. You can be flexible in other ways too. Let clients only see study designs. Or let them edit and create content too. Then there’s the huge range of EDC systems they can choose from. Maximum choice and flexibility.

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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

Values that drive us

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Passion

We love what we do, love our community, and seeing the difference we make for people in the industry.

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Innovation

We’re always adding new stuff – mostly from your feedback. And our product road map promises lots more features to come.

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Integrity

You need us to be honest and clear, and that’s exactly how we are. We do what we say, and if we can’t do something, we’ll tell you.

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Collaboration

We genuinely care about you succeeding, and we’re on your side – think of us as an extension of your team.

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Added value

We get on with things and get them done, no messing. And we’re fast, so you get more done, faster, and get a quick ROI.

FAQs

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.

Start saving time & resource

With automatic processes and built in compliance.