From EDC build and validation to query management, safety data reconciliation, CDISC harmonization, and expert biostatistics — backed by specialized expertise across both human clinical trials and preclinical safety / toxicology environments.
CDMP by NoyMed pairs strict GDPR and HIPAA compliance with transparent pricing, volume discounts, and industry-leading turnaround times.
Swipe or use the controls to move through each pillar.
Software captures your data — it does not manage it. CDMP delivers complete operational execution under one contract, from database configuration to locked, submission-ready datasets.
Part 11 and GCP-validated build, configuration, and validation on TrialKit or legacy environments.
Setup, validation, instrument data integration, and audit-trail management for GLP study environments.
Query resolution, automated checks, safety / SAE reconciliation, and MedDRA / WHODrug coding.
CDISC SDTM/ADaM and SEND datasets in parallel with conduct; full SAS / R programming.
Custom API pipelines for central labs, toxicology equipment, eCOA/ePRO, wearables, and devices.
Platform-to-platform migration, dataset re-architecture, and study rescue in 30 days or less.
Lean clinical and preclinical operations teams looking for rapid decision-making, fast database configurations, and milestone-based billing.
Scale your capabilities with white-label, multi-platform clinical and preclinical EDC expertise and reliable overflow data management capacity.
Specialized non-clinical workflows engineered for automated laboratory instrument data capture and tightening global GLP/SEND standards alongside clinical requirements.
Cost-conscious, fully compliant data management tailored specifically to fit strict grant constraints.
Site-friendly data management setups and direct operational support for sponsor-assigned trials.
CDMP operates on a 21 CFR Part 11, GCP, and GLP-validated foundation. Our delivery hub provides highly efficient, high-tier biometrics execution — guaranteeing dual GDPR and HIPAA compliance alongside extended U.S. time-zone overlap.
Software vendors only sell database or platform access. CDMP provides complete operational execution — handling EDC licensing and full data management, equipment data harmonization, CDISC/SEND mapping, and biostatistics under a single contract. We provide the people and the protocols to run the software.
Contracting is executed via our Netherlands headquarters, ensuring full legal and regulatory alignment under EU and U.S. law.
Clinical database or preclinical configuration go-live is achieved in 1 to 4 weeks depending on study complexity. Study rescue and platform migrations complete in 30 days or less.
Share your study phase, site / laboratory parameters, subject targets, and preferred platform environment. We will deliver a transparent, fixed-fee proposal without lengthy intake cycles.