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Optimized monitoring


Monitoring refers to a rigorous control of the accuracy and completeness of the data collected throughout your clinical trial and that, in accordance with the source documents.
To optimize the implementation of each of your clinical trials, a Clinical Research Associate travels regularly onsite to ensure optimum monitoring throughout your study:

 

  • Qualification visit
  • Initiation Visit
  • Monitoring visit
  • Audit Preparation
  • Inspection visit

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