We can provide customers with audit services for clinical trials, check whether all procedures of clinical trials comply with the requirements of GCP, research protocol, SOP and relevant laws and regulations, find and correct problems in time. In this way, we can protect the rights and interests of subjects and and ensure that the clinical trial data are scientific and reliable.
Familiar with the requirements of ICH-GCP and other relevant regulations, combined with rich clinical audit experience, implement efficient project audit on clinical trials in different fields to ensure the authenticity and standardization of clinical trial operation.At the same time, follow up the implementation of corrective and preventive measures for problems found in the audit.