Risk-Based Pharmacovigilance Auditing and Inspection Preparation

Life Science companies face an increasingly complex set of international regulations in their commitment to patient safety and Good Pharmacovigilance Practice (GVP). For evaluating the performance of the internal processes in a company the use of audits or inspections by external experts is common practice.

Our Concept


We perform and document risk-based audits of your PV system in line with GVP as well as with DIN EN ISO 19011 to guarantee compliance with current legal obligations.
Please do not hesitate to contact us for an individual offer.