SAS & Statistical
SAS & Statistical Programming are at the heart of the work we do at S-cubed. With our team of expert programmers, we have supported the global pharmaceutical industry since 2007. Our consultants can work on site or from our offices, you choose.
Our team of 25+ SAS & Statistical programming specialists have in depth knowledge of the clinical trial process and we can provide comprehensive and effective SAS programming support to the Pharmaceutical and Healthcare Sector.
Our team of expert programmers can support you with all your programming needs including: trial programming, derived data creation, generic macro development, statistician support, TLF production, submission preparation
Data Conversion and Integration
We have extensive experience in legacy and non-standard data conversion and database integration
We were founded on our SAS and CDISC expertise and we can provide comprehensive and effective SAS CDISC programming support for CDISC conversion of legacy and ongoing studies. S-cubed’s programmers and statisticians have converted over 200 studies to CDISC standards.
CDISC Compliance Checking
Having worked with CDISC standards since 2004, we are very familiar with what CDISC issues can typically arise. Based on our extensive experience in performing CDISC conversations and programming, we provide a CDISC checking and compliance service.
Need something specific?
If you require additional support or have a requirement that is not covered here, please get in touch so we can discuss what you need.
Feel Free to contact us,
using the form below!
S-cubed was founded on its CDISC and SAS Programming excellence. We are fully conversant with the requirements for producing SDTM and ADaM in a variety of environments.
General SAS Support
We can offer a variety of consultancy roles and regularly place our experts at pharmaceutical sites. We also offer support and advice on validation and documentation.
CDISC FDA Submission Support
S-cubed’s programmers and statisticians have supported more than 20 successful FDA submissions. We can produce the ISS, ISE and their associated integrated CDISC databases, together with all submission CDISC deliverables (such as Define.xml and Reviewer’s Guides).
CDISC Training and Advice
We are CDISC authorised trainers in SDTM and ADaM. We advise pharmaceutical companies all the way from first steps of implementing CDISC through to full implementation. You can also see our A3 Suite, designed to support implementation of CDISC standards here.