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Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use article 106 CELEX: 02001L0083-20250101 Each Member State shall set up and maintain a national medicines web-portal which shall be linked to the European medicines web-portal established in accordance with Article 26 of Regulation (EC) No 726/2004. By means of the national medicines web-portals, the Member States shall make publicly available at least the following: (a) public assessment reports, together with a summary thereof; (b) summaries of product characteristics and package leaflets; (c) summaries of risk management plans for medicinal products authorised in accordance with this Directive; (d) the list of medicinal products referred to in Article 23 of Regulation (EC) No 726/2004; (e) information on the different ways of reporting suspected adverse reactions to medicinal products to national competent authorities by healthcare professionals and patients, including the web-based structured forms referred to in Article 25 of Regulation (EC) No 726/2004. |