- 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.
