GMP ja ravimite tootmise alane lisateave, viited

EMA - Euroopa Ravimiamet, inspektsioonide rubriik
EDQM - European Directorate for the Quality of Medicines and HealthCare

ICH, VICH (international harmonisation of registration of medicinal products)

European Commission

FDA Center for Drug Evaluation and Research
FDA Office for Regulatory Affairs

Ametite ja riikide koostööorganisatsioonid:

Pharmaceutical Inspection Co-operation Scheme
Pharmaceutical Inspection Co-operation Scheme - Guidance documents (suunatud ravimiametitele, sest PIC/S ühendab ameteid, kuid sisaldavad juhiseid, mida ravimitööstus rakendab)
World Health Organisation - Pharmaceutical Products

GMP ja ravimite tootmise alane info, väljaanded, koolitus:

ECA Academy
International Society for Pharmaceutical Engineering
Parenteral Drug Association
Active Pharmaceutical Ingredients Committee
Institute of Validation Technology
The Center for Professional Advancement
Management Forum
NSF-DBA
Pharmaceutical Quality Group
Institute of Environmental Sciences

Standardid:

European Committee for Standardization
Eesti Standardikeskus