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  • Full GLP compliance (AFSSAPS, AFSSA, COFRAC)
  • Full GMP compliance (authorization Nos. M07/258, AFSSAPS and V2578/07, AFSSA, FDA registration No. 3006118993)
  • Compliance with ICH and VICH guidelines
  • Independent QA Unit
  • Review of protocols / raw data / reports
  • Critical phase inspections
  • Process inspections
  • Monitoring and maintenance of archives for materials and study documentation
  • Internal quality assurance program
  • ISO 14001 Certification (Environment Management System)