GLP (Good Laboratory Practice) Compliance audits are required for non-clinical laboratory facilities conducting safety and toxicology testing in animals including the toxicology facilities and bioanalytical laboratories. These audits will assure the facilities compliance with 21 CFR Part 58. Our auditors can:

  • Perform routine and qualification audits of bioanalytical laboratories 
  • Perform routine and qualification audits of toxicology facilities and laboratories
  • Audit central laboratories
  • Review bioanalytical laboratory data
  • Review toxicology data 
  • Assess data integrity at toxicology and bioanalytical facilities 
  • Assess data transfer process 
  • Perform in-process study inspections

In addition to audits and consulting, we can provide customized on-site training. Click here to learn more.