Clinical Data Management (In pipeline)

We plan to develop flexible, efficient, centralized and coordinated Data Management services for all phases of clinical research in the near future.

We plan to provide the following Data Management services:

• Creation of annotated Case Report Form (CRF) and approval
• Database structure creation and approval
• Data editing plan (Data validation manual) writing and approval
• Edit check programming and testing
• Data listing programming and approval
• Data entry conventions writing and approval
• CRF and queries tracking
• Data processing through double data entry
• Query generation
• Adverse event and medications coding and approval
• Data listing editing and data review
• Serious Adverse Event (SAE) form versus CRF SAE reconciliation
• Electronic batch loading
• Lab data versus sample clinical data verification
• Database quality control
• Database lock and data transfer