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Training
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



