Track Record

Success stories across clinical and preclinical delivery

Representative engagements showing how an integrated data team compresses timelines, holds compliance, and extends partner capacity.

Challenge: A Phase II oncology trial faced a 4-month delay in database launch due to vendor bottlenecks.
Solution: CDMP re-architected eCRFs and completed full GCP validation on TrialKit within 21 days.
Outcome: The study went live ahead of revised enrollment targets, saving an estimated 30% in overall data management costs.

Challenge: An emerging biotech was transitioning from paper records to an electronic preclinical workflow (using Instem Provantis) but lacked the internal data management expertise to configure the platform and map toxicology findings to FDA-mandated SEND formats.
Solution: CDMP's data management team configured the protocol-driven study parameters, set up real-time validation checks for laboratory instrument data capture, and managed the electronic audit trails.
Outcome: The study maintained strict GLP compliance, and all automated toxicology data cleanly integrated into a final SEND-ready submission package on schedule.

Challenge: A mid-tier European CRO required overflow CDISC programming support without expanding internal headcount.
Solution: CDMP delivered parallel SDTM/ADaM conversions under a white-label agreement from our EU / Armenia delivery hub.
Outcome: A clean regulatory submission was achieved on schedule, extending partner service bandwidth seamlessly.

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