As active members of the European CDISC Coordination Committee (e3c) and one of only a few authorised to provide CDISC training, we can assist you in ensuring that your processes and systems conform to CDISC Standards.
The Clinical Data Interchange Standards Consortium (CDISC) was set up to develop and support global, platform-independent data standards, enabling information system interoperability to improve medical research and related areas of healthcare.
The Food and Drug Administration have recommended CDISC (SDTM) standards should be used for electronic submissions of clinical trial data.
Ad hoc Queries - S-cubed's CDISC Specialists can provide answers for all your CDISC Standards questions
Analysis and Input - experienced in conversion and integration tasks, we can support you in planning and implementing all your
CDISC-related projects
Up-to-date Information - by remaining fully informed on all developments in CDISC Standards, we can ensure that you have the most up-to-date information
