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Article R613-25-4 of the French Intellectual Property Code

The arrangements for the identification of products manufactured under compulsory licence pursuant to Article 10-5 of Regulation (EC) No 816/2006 are established by a decision of the Director General of the National Agency for the Safety of Medicines and Health Products.

Original in French 🇫🇷
Article R613-25-4

Les modalités de l’identification des produits fabriqués sous licence obligatoire en application de l’article 10-5 du règlement (CE) n° 816/2006 sont établies par une décision du directeur général de l’Agence nationale de sécurité du médicament et des produits de santé.

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