Clinical Data Management Services
Precision Data Management for Clinical Research
Dileas CS Ltd delivers expert clinical data management services — helping sponsors and CROs bring safe, effective treatments to patients faster.
What we do
End-to-end data management expertise
From study start-up to database lock, we provide end-to-end clinical data management expertise.
Data Management Planning
Comprehensive Data Management Plans tailored to your study protocol, ensuring regulatory compliance and data quality from day one.
Database Build & Validation
Robust EDC database design, build, and validation — delivering clean, audit-ready systems that meet ICH E6 and 21 CFR Part 11 requirements.
Medical Coding
Accurate and consistent medical coding using MedDRA and WHO Drug dictionaries, with rigorous quality review processes.
Data Cleaning & Lock
Systematic data review, query management, and database lock activities — ensuring your data is clean, complete, and ready for analysis.
Strategic Partnership
Dileas CS Ltd and Ancillarie
Dileas CS Ltd partners with Ancillarie to deliver full-service global CRO capabilities. Through this collaboration, we combine Dileas CS Ltd's expertise in Data Management, compliance systems, and technology development with Ancillarie's extensive operational and scientific services.
This partnership allows us to offer sponsors a complete, end-to-end CRO solution while maintaining full independence as separate organisations. Together, we provide scalable delivery from India and governance excellence from the UK — ensuring quality, compliance, and operational efficiency across every study.
Why Dileas?
A partner you can trust
We combine deep expertise with a personal, flexible approach — so your study data is in safe hands.
ICH E6 Compliant
All our processes align with ICH E6(R2) GCP guidelines and regulatory expectations, giving you confidence in your data integrity.
Experienced team
Our team brings years of hands-on clinical data management experience across a wide range of therapeutic areas and study phases.
Flexible engagement
Whether you need full-service DM support or targeted expertise for a specific study phase, we adapt to your needs.
Software by Dileas CS Ltd
Our technology platforms
Logic Line
Coming SoonAI-powered regulatory intelligence — retrieval, inspection analysis, SOP gap review, and structured citations. Built for clinical research professionals.
IDRP
Coming SoonIntelligent Data Review Platform — a compliance-driven, AI-supported data governance system for pharmaceutical, biotech, and clinical research organisations.
Ready to talk DATA?
Let's discuss how Dileas CS Ltd can support your next clinical study. We'd love to hear about your project.