Audit and Inspection in Clinical Research
A systematic and independent examination of trial related activities and documents to determine whether the evaluated trial related activities were conducted and the data were recorded, analysed and accurately reported according to the protocol, GCP and Applicable Regulatory Requirement.
Audit & Inspection
Selection/Audit of CRO as per ICH GCP
Monitoring of Clinical Studies
On-site support during audit/inspection
Regulatory & Internal Audit
CAPA writing & Follow-up with authority till approval
Strategy planning & guidance for regulatory submission