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Altran has developed training modules to guarantee that your resources will receive the most updated knowledge on the industry’s best practices and regulations on the following subjects:

  • Introduction to the GMP: Good Manufacturing Practices for Pharmaceuticals companies
  • ICH Q7: Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
  • Qualification and Validation
  • From Engineering to Validation:
    • V Cycle
    • ASTM 2500 : Pharmaceutical Project Management
  • ICH Q9 : Quality Risk Management
  • 21 CFR Part 11
  • Process Analytical Technology (PAT) & Quality By Design (QBD)
  • ICH Q10