Article L752-1
…e wording resulting fromL. 311-1 Ordinance no. 2013-544 of 27 June 2013 L. 311-2Law no. 2023-171 of 9 March 2023 containing various provisions for adapting to European Union law in the fields of the e…
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Showing 3931–3940 of 32301 articles for “Art. 9 May 2017”
…e wording resulting fromL. 311-1 Ordinance no. 2013-544 of 27 June 2013 L. 311-2Law no. 2023-171 of 9 March 2023 containing various provisions for adapting to European Union law in the fields of the e…
…e wording resulting fromL. 311-1 Ordinance no. 2013-544 of 27 June 2013 L. 311-2Law no. 2023-171 of 9 March 2023 containing various provisions for adapting to European Union law in the fields of the e…
…Credit institutions distributing the savings products referred to in Articles L. 221-1 to L. 221-29 shall provide the Banque de France with the information required to perform its duties at least ev…
Infringement of the prohibitions laid down in Articles 9, 10, 13 and 15 of Regulation (EU) 2017/1001 of 14 June 2017 on the European Union trade mark shall constitute an infringement giving rise to ci…
By way of derogation from the provisions of article R. 5121-99, the registration lapses if it appears that it is not followed by the marketing of the medicinal product on the national territory within…
…erinary medicinal products, in accordance with the amendment envisaged in the version in force on 1 May 2015. Notwithstanding the previous paragraph, a change of registration holder is authorised unde…
…of any country in which the medicinal product is marketed.II. - The Director General of the Agency may at any time ask the registration holder to provide him with any information relating to the volu…
After registration, manufacturing methods and control techniques take account of scientific and technical progress. Any resulting changes must first be registered under the conditions set out in artic…
…n or withdrawal decisions and for the reasons that justify them, the Director General of the Agency may prohibit, as a precautionary measure, the supply of a registered medicinal product, limiting thi…
Registration of homeopathic medicinal products and traditional herbal medicinal products, as well as suspension and withdrawal of registration, are made available to the public by the Director General…
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