Regulatory Audit

We have experience in GCP, GLP and GMP auditing and can undertake both audit and prepare clients for process, vendors and suppliers, clinical trials, manufacturing and regulatory inspections.

 

We can conduct virtual, hybrid and face to face audits and pre-audits depending on requirements.  If findings become apparent, we can work with clients to put plans, processes and procedures in place to reduce non-conformities in a straightforward and agile way, introducing risk registers, trackers and mitigation strategies where appropriate.

 

Please contact us for support and questions in any regulatory matter related to products and medical devices.