The EU GMPs include Chapters 1-9 EU Guidelines to Good Manufacturing Practice Medicinal Products for Human and Veterinary. Includes: Annex 11 - Computerized Systems Annex 15 - Qualification and Validation Annex 16 - Qualified Person and Batch Release Annex 18 - (ICH Q7)Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients Annex 19 - Reference and Retention Samples
