We perform audits at all stages and on all
processes used in the management of clinical trials to assess
adherence and compliance with SOPs, GCP, regulatory requirements,
trial protocol, client instructions and contractual obligations.
Our services include the following types of audit:
Investigational site facilities
Trial data
Trial master files and investigator
site files
Monitoring compliance
Clinical trial documents including the clinical trial
report
We can also provide the following ad-hoc services:
Review of current structure and policies,
processes and documentation
Identification of corrective and preventive
actions for process improvement
Implementation of a comprehensive and
efficient system enabling a consistent quality structure
