Customizable CRF templates, workflow and data validation libraries significantly reduce the development time of your clinical study database.

A typical clinical study database is completed in two weeks, including eCRF design, programming data validation, customizing workflow, testing and documentation. This assumes that a finalized set of template CRFs are available for implementation and no changes to them will be necessary. Similarly, an in-depth, finalized data validation plan should be available, complete enough for implementation / programming. The comprehensive testing and documentation of the core system / functionality of edc^pro in the IT environment of the Clinical Trials Data Center is performed immediately after the publication of a new release / update of edc^pro by Scitek Solutions, Inc.

Main tasks performed include:

• Development of Data Management Plan
• Configuration: Design eCRFs, program data validation and access control / workflow definition; including unit testing
• Configuration testing, documentation, test database
• User acceptance testing - Resolve defects
• Final testing and documentation
• Release study website.

Following production release, site training begins.