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