SMOconnect provides Quality Assurance audits to various sponsors to audit their Indian as well as Global studies.

SMO connect Quality Assurance department consists of a team of experienced QA professionals who can perform on-site monitoring for clinical trials of all phases and can conduct pre-study audits of CROs, investigational site audits, Trial master file (TMF) audits, report audits and system audits, to ensure compliance with Good Clinical Practice (ICH-GCP), FDA and local regulatory standards as a part of clinical trial services.

Internal systems audits include a comprehensive review of procedures and processes followed in the management of clinical trials.