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Medical Consultation


Site Management

Highest Quality, Lowest Risk

Site identification and activation are important components of clinical trials and have critical impact on subsequent trial timelines. ClinActis provides an approach that is expedient and efficient to ensure the highest quality and lowest risk to your trial. Our CRAs are skilled and well-trained in clinical research to deliver the highest quality review of data and effective communication with study sites.

CRA Site Activities

Our CRAs conduct on-site monitoring visits throughout the study to:

  • Oversee data collection

  • Review source documentation and case report forms

  • Ensure regulatory compliance

  • Resolve data queries

  • Conduct interim analyses as requested by the client

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