The Verity Collective brings deep expertise to auditing across the life sciences landscape, with a seasoned network of Subject Matter Experts (SMEs) who have led compliance initiatives at every level. Our professionals have conducted thousands of audits globally spanning GMP, GCP, GLP, GDP, GVP, and BIMO, helping companies identify gaps, mitigate risk, and prepare for regulatory inspections. With former FDA and industry veterans on board, Verity delivers practical, inspection-ready insights that support operational excellence from clinical development through commercial manufacturing.
For Us, It’s All About the Approach
Auditing is essential in today’s fast-paced life sciences environment. But many companies struggle to keep up. Verity’s team of over 50 seasoned auditors brings 30+ years of global experience, covering GMP, GCP, GLP, GDP, BIMO, Ex-FDA, and Mock Pre-Approval Inspections. With experts across the U.S., Canada, and Europe, including Ex-FDA and Qualified Person (QP) auditors, we deliver in-person, remote, or virtual audits tailored to your needs.
We understand that every organization is different. Verity works closely with clients to design and execute audits that fit their goals, from planning and scheduling to reporting and closure. Whether you need full-scale support or a single audit, we’ve got it covered.
GLP Audits
Routine and qualification audits of sponsor and contract laboratories
Routine and qualification of bioanalytical laboratories
Routine and qualification audits of toxicology facilities and laboratories
Critical or in-phase inspections
Audit central laboratories
Review bioanalytical laboratory data
Review toxicology data
Assess data integrity at toxicology and bioanalytical facilities
Procedure or in-process study inspections
GMP Audits
- Vendor/Suppliers
- CMOS
- Drug Product
- API/Drug Substance
- Packaging
- Labeling
- Analytical Laboratories
- Device Manufacturers
- Internal Audits
- Mock PAI Audits
GCP Audits
- Contract Research Organizations (CROs)
- Investigator/Clinical Sites
- Trial Master Fille (TMF/eTMF)
- BIMO (Mock Bioresearch Monitoring)
- REMS (Risk Evaluation and Mitigation Strategies
- Institutional Review Board (IRB)
- Data Monitoring
- Inspection Readiness
