Conducting On-Site Capability Audits
Conducting On-Site Capability Audits How to Conduct On-Site Capability Audits for Clinical Trial Sites Introduction: The Role of On-Site Capability Audits Before initiating a clinical trial at an investigator site, sponsors and CROs must assess whether the site is operationally ready and compliant with GCP and regulatory expectations. While feasibility questionnaires and remote assessments are…