The power of synergy: why CDMP was created
Traditional setups isolate software from service. We do the opposite.
A spin-off built around repeatable needs
As a strategic spin-off of Streamlined Lean Solutions, CDMP by NoyMed was born out of a clear market necessity. We noticed that certain types of organizations — emerging biopharma, niche CROs, preclinical facilities — have repetitive, predictable data needs. NoyMed can improve the time, cost, and quality of the overall solution and delivery by combining our services with systems into single, simple packages for sponsors and CROs.
By seamlessly blending expert data management workflows with agile EDC systems into a single, unified package, we bridge the gap between technology and execution. The result: we dramatically optimize timelines, lower operational costs, and elevate data quality for both standard protocols and niche study types.
What "one accountable team" means in practice
- One contract: EDC licensing, data management, coding, biometrics, and closeout under a single agreement.
- One team: preclinical LIMS/EDC config, clinical data cleaning, and CDISC/SEND programming report through the same group — nothing drifts between handoffs.
- One standard: a 21 CFR Part 11, GCP, and GLP-validated foundation with dual GDPR and HIPAA compliance.
- Predictable economics: value-based rate cards below traditional U.S. and Western European CRO benchmarks, with volume discounts for recurring portfolios.
Aligned to EU and U.S. law
Contracting is executed via NoyMed's Netherlands headquarters, ensuring full legal and regulatory alignment under EU and U.S. law. Delivery runs from our EU / Armenia hub with extended U.S. time-zone overlap.