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Article R5141-47-10 of the French Public Health Code

In specific cases of Community interest, the Director General of the Agence nationale de sécurité sanitaire de l’alimentation, de l’environnement et du travail or the applicant shall refer the matter to the European Medicines Agency for application of the Community arbitration procedure before a decision is taken on the granting, variation, suspension or withdrawal of the marketing authorisation, in particular on the basis of pharmacovigilance data.

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Article R5141-47-11 of the French Public Health Code

When the Director General of the Agence nationale de sécurité sanitaire de l’alimentation, de l’environnement et du travail considers that the variation, suspension or withdrawal of a marketing authorisation which he has granted following a mutual recognition or decentralised procedure is necessary for the protection of human or animal health or the environment, he shall immediately inform the European Medicines Agency for the application of the Community arbitration procedure. In…

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Article R5141-47-12 of the French Public Health Code

At the end of the Community arbitration procedure implemented in accordance with the provisions of Articles R. 5141-47-9 to R. 5141-47-11, the Director General of the Agence nationale de sécurité sanitaire de l’alimentation, de l’environnement et du travail shall grant, vary, suspend or withdraw the marketing authorisation within a period of thirty days, in accordance with the decision taken by the European Commission at the end of this procedure.

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Article D5141-55 of the French Public Health Code

I.-The amounts of the fee provided for in 1° of 1 of I of Article L. 5141-8 for marketing authorisation applications under a national procedure, a mutual recognition procedure or a decentralised procedure for which France acts as the reference Member State are set as follows: 1° €25,000 for an application relating to : a) A veterinary medicinal product which is the subject of a complete dossier referred to in…

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Article D5141-55-1 of the French Public Health Code

I.-The amount of the fee provided for in 8° of 1 of I of Article L. 5141-8 is set at €1,500 per veterinary medicinal product or per series of homeopathic veterinary medicinal products and forming the subject of the dossier referred to in Article 87 of Regulation (EU) 2019/6 of the European Parliament and of the Council of 11 December 2018 on veterinary medicinal products and repealing Directive 2001/82/EC. II….

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Article D5141-56 of the French Public Health Code

I.-The amount of the fee provided for in 2° of 1 of I of Article L. 5141-8 for a variation to a marketing authorisation requiring an assessment as part of a national procedure or a mutual recognition procedure for which France acts as the reference Member State is set at €5,000 and €1,000 per additional medicinal product. II. The amount of the fee provided for in 2° of 1 of…

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