Expedite the delivery of submission ready datasets with expert support during clinical trials.
Compliance with Clinical Data Interchange Standards Consortium (CDISC) standards during clinical trials reduces the time to regulatory submission and enables better communication between team members.
Comprehensive CDISC expertise and consultancy
We provide extensive CDISC expertise and consultancy solutions through our biometrics specialists and we are an official CDISC Registered Solutions Provider (RSP) for Study Data Tabulation Model (SDTM), Analysis Data Model (ADaM) and Define.xml.
Our experts will ensure you receive early access to SDTM datasets to guide your trial through its initial stages. With validated in-house software, we ensure CDISC compliance for your dataset utilizing a metadata repository approach that delivers high quality CDISC deliverables.
Should you need customized assistance, we can support you with a variety of flexible legacy data services, including the development of CDISC implementation guides (IG) for SDTM, ADaM, Define.xml and metadata repository creation and maintenance.
Whatever your requirements, we have the CDISC expertise to help.
Why choose SGS?
We are recognized as the benchmark for quality and integrity in clinical trials. Our experts have successfully supported multiple clinical trial submissions to global authorities.