Clinical Trial Site Monitoring for Ongoing Compliance

Our independent monitoring services ensure that clinical trial sites comply with all regulatory requirements and maintain data integrity throughout the trial.

Why Site Monitoring is Important

Site monitoring ensures the trial is conducted in accordance with the approved protocol, GCP, and regulatory requirements, safeguarding the rights and safety of participants.

What We Monitor

Informed Consent Documentation
erence to Protocol
a Collection & Integrity
Investigational Product Accountability
Reporting of Adverse Events (AEs) and Serious Adverse Events (SAEs)

Monitoring Process

Initial Consultation
On-Site Visits & Remote Monitoring
Documentation Review
Compliance Reporting
Follow-Up Support

Ensure Trial Integrity with CRET

Partner with us for professional, independent site monitoring to ensure trial compliance and data integrity.