ethica can design your Case Report Form (CRF) directly from the study protocol and/or a set of standardized modules. The proper protocol interpretation and selection of analytical variables are ensured through timely interactions between Clinical Research, Statistics, and Data Management departments. A thorough review is performed to ensure consistency, completeness, and data integrity. The final result is a streamlined CRF that provides a perfect balance between user-friendliness and data processing requirements.

ethica provides complete flexibility for the format of the final CRF. CRFs can be printed in a traditional manner or they can be optimized for fax-based processing. Alternatively, your CRF can be structured by our experts for electronic data capture.