欧盟:
Eudralex(European Union Law On drug regulatory affairs)
Vol 1: Legislation Human
Vol 2: Notice to Applicants Human
Vol 3: Guidelines Human
Vol 4: GMP Human & Veterinary
Vol 5: Legislation Veterinary
Vol 6: Notice to Applicants Veterinary
Vol 7: Medicinal Products Veterinary
Vol 8: MRL Veterinary
Vol 9: Pharmacovigilance Human & Veterinary
Vol 10: Clinical Trials
Vol 1和Vol 2是法律,Vol 3至Vol 10是法规或指南。
其中,Vol 4就是GMP,其母法就是第一卷中的“Directive 2003/94/EC for medicinal products and investigational medicinal products for human use”
美国
Code of Federal Regulations其中第21篇就是“食品与药品”,也就是我们常说的21 CFR。本篇共有9卷、3章、1499部。其中,第4卷第1章第C分章210和211部就是CGMP.CGMP是法律。