European legislation requires the Marketing Authorisation Holder (MAH) to perform regular risk-based audits of their pharmacovigilance system. Our experienced team provides auditing services aiming to ensure that all relevant documentation and procedures are in place and in compliance with current legislation as well as identifying process/quality improvements. We can also provide assistance during pharmacovigilance inspections, development of CAPAs, and dealing with critical and/or major findings. Visit: Pharmacovigilance Audit