Clinical Trial Monitoring

The highest quality review of data and effective interaction with study sites are the top priorities of our clinical operation team during on-site monitoring visits. 

To provide you with the most reliable data we work with the sponsor to continuously update the Monitoring Plan throughout the study and, based on factors like patient enrollment, data entry and query resolution trends, site training needs, and observed site issues, adapt the frequency of planned site visits. 

Key activities

  • Monitoring Plan Design

  • Monitoring Section of Protocol

  • Initiation, Monitoring & Closing Visits

  • Telephone conferences

  • Resolution of Data Clarification Forms (DCF) with Sites