With EEA-Lex you can find information about proposed EU legal acts with possible EEA relevance, adopted EU acts under consideration for incorporation into the EEA Agreement, and acts that have already been incorporated into the Agreement.
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D050582/03
Commission Directive (EU) 2017/1572 of 15 September 2017 supplementing Directive 2001/83/EC of the European Parliament and of the Council as regards the principles and guidelines of good manufacturing practice for medicinal products for human use
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Richtlinie (EU) 2017/1572 der Kommission vom 15. September 2017 zur Ergänzung der Richtlinie 2001/83/EG des Europäischen Parlaments und des Rates hinsichtlich der Grundsätze und Leitlinien der Guten Herstellungspraxis für Humanarzneimittel
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Tilskipun framkvæmdastjórnarinnar (ESB) 2017/1572 frá 15. september 2017 um viðbætur við tilskipun Evrópuþingsins og ráðsins 2001/83/EB að því er varðar meginreglur og viðmiðunarreglur um góða framleiðsluhætti við gerð mannalyfja
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Kommisjonsdirektiv (EU) 2017/1572 av 15. september 2017 om utfylling av europaparlaments- og rådsdirektiv 2001/83/EF med hensyn til prinsipper og retningslinjer for god framstillingspraksis for legemidler for mennesker
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