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Formedix

Formedix

Want to design and build clinical trials faster with less effort?

Now you can, with our new clinical metadata repository (CMDR) and automation cloud platform, ryze. We've automated manual, labor-intensive processes, and given you the tools to standardize study build and integrate 3rd party platforms.

Simply house your standards and study library in the central MDR, then easily find, manage, and reuse content. Even import content from EDCs and e-clinical systems into ryze.

You can design studies for leading EDCs - and see exactly how forms look in ryze without having to build your study. Instantly convert datasets to SDTM, and make submission deliverables with the click of a button. And all effortlessly in line with CDISC standards.

ryze is built on CDISC compliant templates, so compliance is enforced throughout study build. Plus, ryze is a cloud-based off-the-shelf suite, so there's zero install and it's ready to go when you are!

Related resources

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SDTM supplemental qualifiers explained

SDTM supplemental qualifiers explained

Content provided by Formedix | 12-May-2023 | White Paper

What are SDTM supplemental qualifiers? In short, these are variables in non-CDISC datasets that cannot be mapped to a variable that matches the SDTM standard....

How clinical trial software can optimize trials

How clinical trial software can optimize trials

Content provided by Formedix | 17-Apr-2023 | White Paper

Companies often have to conduct multiple clinical trials at the same time, which means they've got to be efficient, and compliant with industry regulations....

ODM and CDASH in CRF design

ODM and CDASH in CRF design

Content provided by Formedix | 10-Mar-2023 | White Paper

The lesser-known Operational Data Model (ODM) standard is often overlooked as it's not required by any regulators. So, why should you be interested...

Standardizing data with NCI controlled terminology

Standardizing data with NCI controlled terminology

Content provided by Formedix | 13-Feb-2023 | White Paper

The use of consistent terminology within and between studies is critical to enabling an efficient trial process. CDISC standards such as CDASH, SDTM, SEND...