GMP ja ravimite tootmise alane lisateave, viited

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

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
Scottish Society for Contamination Control

Standardid:

European Committee for Standardization
Eesti Standardikeskus