Data Management

Our data-managers are part of the team to make a medical device study a success. They actively participate in the design and implementation of a trial, using their vast experience and specific medical device knowledge to serve the goal of the study. Whether they help Principal Investigators and study nurses who prefer paper/digital CRFs or full EDC, they will adapt their process to guarantee that a clean database can be locked almost immediately (days, not months) after Last-Patient-Last-Visit.Our data-management activities consist of:

  • CIP design
  • CRF design
  • Database design and validation
  • Electronic Data Transfer Design
  • Discrepancy Management
  • Database Quality Control
  • Data Coding
  • Data conversion programming
  • Database lock