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Council Directive 75/318/EEC of 20 May 1975 on the approximation of the laws of Member States relating to analytical, pharmaco-toxicological and clinical standards and protocols in respect of the testing of proprietary medicinal products · European Union

un ' indicazione delle varie fasi della fabbricazione che consenta di valutare se i procedimenti impiegati per realizzare la forma farmaceutica non abbiano potuto dar luogo ad alterazione dei componenti ;

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Source: EUR-Lex (Cellar) · retrieved 2026-11-10 · Text as adopted (Official Journal); later amendments are not incorporated in this text.