Hivatkozások

• Androvera Consulting Hungary
• CHMP members
• EBE : European Biopharmaceutical Enterprises
• GphA  : Generic Pharmaceutical Association
• CHMP Pharmacovigilance Working Party
• Electronic Common Technical Document (eCTD)
• Change Control Process
• ICH
• TOPRA
• MedDRA
• Parallel imports of proprietary medicinal products
• The single market in pharmaceuticals
• Strengthening the European pharmaceutical industry for the benefit of the patient
• Good laboratory practice: tests on chemical substances 
• Good laboratory practice: inspection and verification
• Supplementary protection certificate for medicinal products
• Community code: medicinal products for human use
• Medicinal products for paediatric use
• Prices: pricing and health insurance
• Good clinical practice
• Orphan medicinal products
• Pharmaceutical committee
• Community patent
• Patent law in the field of biotechnology and genetic engineering: Commission report
• Agreement on intellectual property rights relating to trade and pharmaceutical patents
• Enterprise Directorate General - Pharmaceuticals
• European Pharmacopoeia
• European Chemicals Agency (ECA)
• European Centre for Disease Prevention and Control (ECDC)
• European Translation Centre (ETC)
• European Monitoring Centre for Drugs and Drug Addiction (EMCDDA)
• Electronic Medicines Compendium
• Office for Harmonisation in the Internal Market (Trade Marks and Designs) (OHIM)
• World Health Organization
• WHO
• WHO International Database
• EudraVigilance
• The International Society of Pharmacovigilance
• The official journal of the International Society of Pharmacovigilance
• Innovatív Gyógyszergyártók Egyesülete
• European Directorate for the Quality of Medicines
• EudraLex
• EGA
• Az Orvos-Világszövetség Helsinki deklarációja
• The World Medical Association
• Association of the European Self-Medication Industry (AESGP)