Independent Quality Oversight
We execute rigorous vendor audits across the whole GxP spectrum, QP audits, due diligence audits for investors and insurance companies, internal gap analyses, and mock inspections mimicking authentic agency protocols.
Farbridge’s team of former FDA investigators and EMA/MHRA inspectors help your team prepare for regulatory inspections by providing training sessions, interactive role play activities, and by performing full-blown mock inspections (hats on/hats off or with a debrief at the end).
Farbridge has experience supporting remediation activities (e.g. FDA warning letters and 483s).
We Train Your Auditors
Auditing: get hands-on training from our auditors while they audit your Quality Management System or accompany them at your suppliers’.
Our auditor training is a bundle of theory and practice: the theory through our pre-recorded GxP Academy module on the LMS, and the practice alongside our auditors during internal audits at your facilities and audits of your vendors.
Explore the GxP Academy ➔Our Audit Services
We have conducted countless audits around the world.
Our auditors have been carefully selected for their specialized knowledge in various regulations and technical fields. They are strategically positioned across key geographic regions, allowing us to serve you with your audit needs anywhere in the world.
- Quality Audits (Qualification, Routine and For Cause Audits)
- Due Diligence Audits (e.g., before Merger and Acquisition, on behalf of insurance companies, etc.)
- Mock Inspections (US FDA, EMA, MHRA, Swissmedic, Health Canada, TGA, ANVISA, NMPA) by Senior Auditors or former Health Authorities Investigators/Inspectors
- European Qualified Person (QP) Audits
- Australian Authorized Person (AP) Audits
- Experience across all GxP, including audits of Service Providers (such as Contract Development and Manufacturing Organizations (CDMOs), Contract Research Organizations (CROs), Third-Party Logistics (TPLs), GCP Clinical Labs, GMP QC Labs, GLP In Vitro Testing Labs, Vivarium Labs, Pharmacovigilance Service Providers, Market Research Agencies, Regulatory Affairs Consulting firms, etc.), Clinical Sites, Suppliers, Blood Banks, GPP medicinal cannabis suppliers, GACP Medicinal plants suppliers, Commercial Partners, etc.
Talk to an Audit & Inspection Readiness Specialist
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What Happens Next
1. We review your inquiry within 1 business day.
2. A specialist scopes your engagement.
3. You receive a tailored proposal.