- Validate against relevant CDISC standards required by the FDA.
- Be automatically prompted to fix errors if you stray from CDISC standards.
- Fix any errors early (with our rule based templates).
- Easily compare studies against specifications or against organizational standards.
- Validate CRFs against clinical expectations.
- Validate EDC design against CRF specs.
- Validate EDC datasets against specs.
- Validate SDTM datasets against CDISC standards (SDTM-IG, NCI Controlled terms etc).
- Validate SDTM programming.
- Validate SDTM clinical data against CDISC SDTM, NCI standards and FDA or PMDA rules.
- Validate ADaM datasets.
- Validate SEND.
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.
