Monday - Saturday, 8AM to 10PM

To improve the quality and validity of test data, GLP is required for all laboratories and research institutions to evaluate the safety or effectiveness of chemicals. Good Clinical Laboratory Practice (GCLP) ensures achievement of the goals of the GCP principles. It applies to the principles established within the framework of the GLP. Our team of auditors has active certification and in-depth knowledge of relevant best practices in accordance with the OECD Principles of Good Laboratory Practice. Our GLP team has the experience and ability to conduct audits of all types, including facilities; data processing; Research specific data and reports against GLP requirements. We test central laboratories and bioanalytical laboratories to perform routine and specialized analyzes in accordance with GLP and GCP regulations. Our range of GLP/GCLP services include:

  • Critical or in-process Phase InspectionsCritical or in-process Phase Inspections
  • Bioanalytical Lab Auditss
  • Protocol Audits
  • Facility Auditss
  • Report Audits
  • Process/Procedure Audits
  • Qualification and Re-Qualification Audits
  • Archive Audits
  • Mock Inspections
  • Study Audits
  • GLP/GCLP gaps analysis
  • Document Reviews
  • Data Integrity Assessments
  • Subcontractor and Vendor Audits