Auditing Services
Auditing is an essential requirement for organizations as the life science landscape continues to expand. Many companies struggle with the balance required to develop audit schedules, find qualified individuals to conduct audits, and complete the audits in a timely manner. Verity’s team members have been conducting audits for over 30 years both nationally and abroad. With over 50 auditors dedicated to conducting independent evaluations of external or internal sites there is no audit too complex for our team to handle.
Verity’s primary auditing focuses are: GMP, GCP, GLP, GDP, Ex-FDA, BIMO and Mock Pre-Approval Inspections. Our auditors are located in the US, Canada, and Europe. All audits can be conducted in-person, remote or virtual as required. We have EX-FDA and Qualified Person (QP) Auditors in our network as well.
For Us, It’s All About Approach
We understand that one size does not fit all and work with our clients to understand their specific needs and requirements for a successful outcome. With our extensive resources we can be as hands-on or hands-off as a project requires. This may entail activities such as identifying the audit sites, creating audit plans, scheduling the audits, developing agendas, providing templates, conducting the audit, and closing the audit with reports or summaries of findings.
Learn More About Our Capabilities
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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 -
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