Quality Auditing & Audit Reports

PharmaLex quality specialists have more than 30 years’ experience auditing drug development vendors for GXP standards.

  • Contract Research Organizations (Nonclinical GLP and Clinical GCP)
  • Clinical Sites (GCP)
  • Contract Manufacturing Organizations (cGMP)
  • Analytical Laboratories (GLP/GMP)
  • Bio-Analytical Laboratories (GLP/GCP)