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That’s what you can expect when you start using our study automation platform.
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.
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.
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.
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.
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.
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.
We’re using the Formedix platform to design CDASH example CRFs for the CDISC CDASH-IG standards package. We can create, visualize, edit and approve eCRFs in the platform, then export them in ODM-XML to use in the CDISC Library and standards packages. Formedix is one of CDISC’s longest standing members. CDISC is keen to work with technology partners that help pharmaceutical organizations to adopt and keep pace with emerging CDISC standards.
Formedix has been a valuable resource and their services have added value to our platform and data management capabilities.
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.
We love what we do, love our community, and seeing the difference we make for people in the industry.
We’re always adding new stuff – mostly from your feedback. And our product road map promises lots more features to come.
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.
We genuinely care about you succeeding, and we’re on your side – think of us as an extension of your team.
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.
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.
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.
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!
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.
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.
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.