EU legislation and regulation documents
EU pharma milestones - European Commission
General basis for market authorisation of medicinal products
Expands general basis of Directive 65/65/EEC (The manufacture, control, supervision, import and export rules were later on also binding for homeopathic and anthroposophic medicinal products later Directive 92/73/EEC refers to 75/319/EEC)
75/318/EEC
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