Clean Data. Confident Decisions. Accelerated Outcomes.
In clinical research, data isn’t just information — it’s insight, evidence, and the foundation for every regulatory decision. Our CDM team ensures your data is accurate, consistent, and submission-ready.
Why This Service Matters
High-quality data is essential for regulatory approval and patient safety. We deliver clean, audit-ready datasets using global standards and flexible delivery models.
Our Key Capabilities
End-to-end clinical trial management you can trust
📋 Database Design & Build
- CRF/eCRF development
- EDC platform configuration
- Edit checks & validation
- CDASH/CDISC/SDTM mapping
🏢 Data Collection & Validation
- Data entry & discrepancy management
- Query resolution workflows
- SAE reconciliation & medical coding
🧠 Review & Reconciliation
- Vendor data reconciliation
- Data trend analysis
- Pharmacovigilance data integration
📦 Database Lock & Submission
- Data QC, freeze, and lock
- SDTM/ADaM dataset export
- Submission package preparation
🩺 Therapeutic Area Expertise
- Oncology
- CNS & Psychiatry
- Infectious Diseases
- Cardiometabolic Disorders
- Rare & Orphan Diseases