For the TIG Product Impact on Individual Health use case, the following assumptions are common to the FT and QS domains as well as the Clinical Classifications use case of the RS domain.
All standard QRS supplement development is coordinated with the CDISC SDS QRS Subteam as the governing body. The process involves drafting the controlled terminology and defining instrument-specific standardized values for qualifier, timing, and result variables to populate the SDTMIG FT, QS, and RS domains. These supplements are developed based on user demand and therapeutic area standards development needs. Sponsors should always consult the CDISC website to review the terminology and supplements prior to modeling any QRS instrument.
- Sponsors may participate and/or request the development of additional QRS supplements and terminology through the CDISC SDS QRS subteam and the Controlled Terminology QRS subteam.
- Once generated, the QRS supplement is posted on the CDISC website (https://www.cdisc.org/standards/foundational/qrs).
- Sponsors should always consult the published QRS supplements for guidance on submitting derived information in SDTMIG-based domains.
- Sponsors may participate and/or request the development of additional QRS supplements and terminology through the CDISC SDS QRS subteam and the Controlled Terminology QRS subteam.