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Increase the speed and quality of clinical studies from design to submission with Formedix ryze – the cloud-based Clinical Metadata Repository (CMDR) and automation suite. Now you can build CDISC compliant studies in 6 weeks or less! And because our clinical trial software is off-the-shelf, you can start straightaway!
Metadata is stored in one central place, so it’s quick to find what you’re looking for and easy to collaborate.
Never build studies from scratch again! Reuse metadata content in ryze – regardless of your EDC – and save time and effort on study setup.
See what forms look like for your EDC in ryze without having to build your EDC – enabling quicker review-approval cycles.
Once approved, it’s 1 click to build your full EDC study from standards in ryze – including edit checks and visit schedules. We support all the leading EDCs, so take your pick or mix and match. And if it’s Rave or Clinical One, you can instantly import studies back into ryze to make changes. Saving time on study build means trials can start much sooner!
Save time and effort on compliance when you build studies in ryze. The platform is built on the latest CDISC compliant templates, including NCI CT.
ryze predicts what your source dataset column headings will be during study design. Then our mapping tools help you map source datasets to CDISC SDTM. Now you know that you’ll collect all the relevant data, and when trial data is ready, your datasets are already mapped!
Once you’ve got your mappings, ryze lets you run SDTM conversions from 1st patient in. Now you can instantly see trial data and make informed safety and efficacy decisions much sooner than before. Plus, ryze gives you all the file formats you need, including SAS Transport v5 (.xpt), dataset-XML and CSV.
The ryze metadata repository and clinical trial automation platform will help you design, build, and submit your trials much faster than before.
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Company number SC159080