Our programmers are actively involved with CDISC initiatives and working groups giving them access to the latest standards. We have a proven track record of implementing complex CDISC mappings for many clients across pharma, biotech, academia and medical devices.
Standardizing data into CDISC format is a difficult and time-consuming task requiring expert skills and specialist experience to ensure your study meets all the requirements for submission.
Our dedicated team of CDISC specialists have combined experience in SDTM, ADaM and associated documentation so no need for separate teams for standardization or analysis. They work across all CDISC standards and have supported many clients with submission efforts to regulatory authorities.
