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Sanjeevani employs traditional methods as well as internet-based solutions to prepare your CRF and ultimately manage the collection, QC and QA of the data during the trial.

CRF and eCRF design
Data management plan development
Data collection system development, including database design, programming, validation and system maintenance
Orientation/Initiation Visits, including Verification, Collection of regulatory documents and discussion of trial parameters
Interim monitoring visits, including source data verification, IRB / SAE document review and CRF corrections
CRF processing, including tracking, double data entry and verification
Electronic data collection
Data cleaning / Quality Assurance, including edit checks, query resolution and documentation of corrections
Medical coding
Reconciliation of external data