What is CDISC and why is it important?

CDISC (Clinical Data Interchange Standards Consortium) provides global standards for clinical research data. Standards like CDASH, SDTM, and ADaM are required by regulatory agencies (FDA, EMA) for drug submission data.

Who should take CDSA courses?

Our courses are designed for Clinical Data Managers, SAS/R Programmers, Biostatisticians, Clinical Research Associates, and anyone working with clinical trial data in pharma, biotech, or CRO environments.

Are CDSA courses recognized by employers?

Yes. CDSA courses are aligned with CDISC standards and taught by industry experts from top pharmaceutical companies and CROs. Our graduates work at AstraZeneca, Pfizer, IQVIA, Parexel, Covance, and more.

What formats are available for training?

We offer three formats: Online Learning (self-paced), Virtual Live Training (interactive sessions), and In-Person Live Training at our Belgium facility.

How long are the courses?

Courses range from 24 to 48 hours of instruction, typically delivered over 2-3 days for live sessions or spread over several weeks for self-paced online learning.