Using validated and industry standards 21CFR compliant systems for paper and EDC trials, our CDM services includes

1. End to end clinical data management for paper and EDC studies
2. Creation of data management plan and Preparation of edit check documents

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3. e (CRF) design
4. Annotation of CRFs
5. Database design, testing and validation
6. Scanning and Indexing
7. Data entry and discrepancy management
8. Data Integration
9. Medical Coding
10. Automatic and manual medically supervised generation of DCFs
11. QC, Database lock and transfer
12. EDC validation and programming
13. Site assessment for EDC
14. Training and support/ Helpdesk
15. Tracking and reporting including customer reports

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