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CLINICAL DATA MANAGEMENT

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

OUR SERVICES