Create compliant ADaM datasets faster and avoid delays in submission

• See what source dataset variables will be much earlier– well before you’ve got any patient data (our platform predicts what they’ll be)
• Map source datasets to target datasets before you’ve got patient data – using the mappings and templates in our platform (no coding)
• Map ADaM datasets back to SDTM with our user friendly mapping framework
• Convert datasets to SDTM in 1 click as soon as you get trial data (run data conversions automatically, daily if needed, and enable real-time clinical data insights)
• Cut time from first patient data to SDTM  by at least half – get SDTM in 4 weeks or less
• Easily comply with earlier versions of CDISC standards required by the FDA – they’re embedded in our platform
• Use our templates to create datasets that comply with ADaM standards, SDTM standards, CDASH, SEND, & Define-XML
• Use our templates to add domains and variables that are automatically compliant with CDISC standards
• Add additional compliant metadata, such as supplemental qualifiers, derivation methods and value list metadata
• Reuse metadata assets, such as ADaM datasets, by creating organizational standards – increase quality, consistency and save time

Sound good?

There’s no obligation, so why not book a demo now and see how better off you could be with ryze!

Complete the form below to arrange your clinical trial software demo.