Article L6433-1
…3-1 are applicable to Wallis and Futuna in the wording resulting respectively from Law no. 2023-379 of 19 May 2023 on improving access to care by trusting healthcare professionals and Law no. 2016-41…
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Showing 3731–3740 of 57608 articles for “Art. Decree 2023-1007 of 30-10-2023”
…3-1 are applicable to Wallis and Futuna in the wording resulting respectively from Law no. 2023-379 of 19 May 2023 on improving access to care by trusting healthcare professionals and Law no. 2016-41…
Any professional who disregards the prohibitions set out in 1° to 3° of article L. 121-23 is punishable by an administrative fine of up to 15,000 euros for a natural person and 75,000 euros for a lega…
An administrative fine of up to €15,000 for a natural person and up to €75,000 for a legal person shall be imposed for failure to comply with the provisions of Regulation (EU) 2018/302 of the European…
Where, in exceptional circumstances, certain provisions of this sub-section encounter difficulties in application, the Minister for the Interior and the Minister for Health shall provide for them by m…
The provisions of article R. 4113-110 are applicable, when they are not members of the health professions, to members of the boards and committees sitting with the Agency and to persons occasionally c…
The parallel import authorisation is granted for a period of five years. It specifies the differences mentioned in articles R. 5121-117 to R. 5121-119 with the speciality that has obtained marketing a…
…only import a medicinal product in a quantity compatible with personal therapeutic use for a period of treatment not exceeding three months under normal conditions of use, or for the period of treatme…
The application for renewal of the parallel import authorisation must be submitted no later than three months before the expiry date of the parallel import authorisation. It must be accompanied by a d…
The certificates referred to in Article L. 5124-11 are issued by the Director General of the Agence nationale de sécurité du médicament et des produits de santé. These certificates are valid for three…
…met: 1° The proprietary medicinal product is obtained from an authorised company within the meaning of Article 77 of Directive 2001/83/EC of the European Parliament and of the Council of 6 November 20…
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