Audit and Inspection in Clinical Research

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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