Working towards "State-of-the-Art" within Pharmacovigilance


Let Audit PV be your preferred partner


Audit PV was launched to provide a specialist consultancy service that is able to support organisations globally in order to develop a "State-of-the-Art" pharmacovigilance system.


We aim to provide specialist expertise in GVP, GCP and IT through activities such as auditing and inspection readiness; development and further enhancement of your quality management system, QPPV/ Deputy QPPV services and clinical support.

Audit PV achieves this by partnering with organisations which we believe to be of the highest calibre within the industry and that we can endorse.

History and philosophy

Audit PV is a start-up company launched in 2013 with the aim to provide quality expertise in pharmacovigilance and quality management services to organisations in an increasingly regulated GxP environment that is both cost-effective and suitable for the identified needs.

Based in Greater London but having a global reach the Audit PV team aims to approach each project in such a way that the final output is "state-of-the-art" and mirrors the expectations of regulators worldwide.

Audit PV ensures that it has a work ethic which works to the highest quality standards. We do this by constantly reviewing our progress and engaging each client to identify milestones and ensure that key achievements are met on time throughout each project and on budget.



The experience within Audit PV covers several years in the fields of pharmacovigilance and quality assurance. Our team members have held positions in organisations ranging from senior pharmacovigilance officers through to EU-QPPV.


In addition to ensure that we are able to provide a completely rounded service; Audit PV is partnered with specialised consultants globally in order to provide expertise in all areas that may be of interest to potential clients.