Reuse studies & standards and build studies in 6 weeks or less with ryze Clinical MDR

Book a free demo and see how to:
  • Store and govern clinical data standards and study metadata in 1 place – standards, forms, datasets, mappings, edit checks, terminologies…
  • Search for metadata in 1 place and instantly find content – a Single Source of Truth.
  • Manage and share metadata content across global teams.
  • Set up and maintain CDISC compliant standards (our platform has templates for all versions of CDISC standards required by the FDA).
  • Reuse all metadata content – set up studies faster and improve consistency.
  • See how eCRFs will look and work for your chosen EDC as you design forms in ryze – without having to build your EDC.
  • Manage organizational standards through their full clinical lifecycle.
  • Control changes to standards and studies – set author-review-approval-production processes.
  • Define rules for change/review cycles.
  • Instantly see change reports and easily track versions of metadata content across their lifecycle.
  • Instantly see the impact of any potential changes before you make them.
  • Easily transfer metadata between our MDR and your systems with our API.

Sound good?

There’s no obligation, so don’t delay! Book a demo now and see how you could be better off with ryze Clinical MDR and automation suite.

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
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