Effective clinical data management (CDM) is at the core of any successful clinical trial. At Clincorp Technologies, we’ve made the collection and handling of clinical trial data a central part of our entire service offering. Clincorp Technologies CDM team leaders have more than 12 years of experience, on average, and a background in medicine or biological sciences. Each has experience in multiple therapeutic areas and in handling data needs for local, regional and global trials.

CDM services are available as part of our integrated service offering or under a complete or partial Functional Service Provider (FSP) relationship. Our global staff uses our well-documented processes and service levels agreements to ensure timely deliverables. We handle all phases of clinical research across the full spectrum of therapeutic areas.

Our Team has many years of Industry experience working with two fully validated clinical data management systems – Phase Forward’s Inform Architect and Oracle Clinical & RDC – as well as working on our customers’ systems provided by other vendors. Clincorp Technologies can provide complete data management for your project or individual services as needed:

• CRF page tracking!
• CRF design
• Database design and programming
• Integration of data from other sources
• Coding
• Data validation
• Status and tracking reports
• Patient related outcomes
• SAE reconciliation
• Electronic Data Capture
• Paper CRF studies
• Double data entry
• Data coding and cleaning
• Validated electronic edit checks
• Support for EDC and Paper CRF's
• Creating SAS Data extracts