ClinTech Research provides a unique clinical data management outsourcing offering to our clients by combining technical project management and study coordination from US with clinical data processing & offshore clinical trial data entry from India. We are uniquely positioned to provide following data management services in the regulatory environment because of our global SOPs, US FDA 21 CFR Part 11 compliance and Computer System Validation & Implementation experience within the US industry:

• Data Management Plan (DMP)
• Database Design & Setup
• Edit Checks Programming & Validation
• CRF Management using a Validated Indexing & Tracking system
• Validated Manual Double Data Entry
• Central Lab Data Import
• Medical/AE Coding
• Query Management
• Manual Data Quality Control (QC)

We have a flexible Data Management service offering to suit our client's specific needs. We can perform Data Management using your existing system or our Clinical Data Management system. We have experience with Oracle Clinical and various EDC systems. In addition, using our offshore and onshore business model, we can offer our clients maximum return on their investment (ROI) both in terms of value and quality.