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Article R5141-41 of the French Public Health Code

The Director General of the Agence nationale de sécurité sanitaire de l’alimentation, de l’environnement et du travail may automatically vary a marketing authorisation for a veterinary medicinal product in order to restrict the indications, limit the conditions of supply, change the dosage, add a contraindication or any other preventive measure when it appears : 1° Either, in particular following evaluation of the data mentioned in article R. 5141-90, that the…

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Article R5141-42 of the French Public Health Code

The Director General of the Agence nationale de sécurité sanitaire de l’alimentation, de l’environnement et du travail may also suspend, for a period not exceeding one year, or revoke a marketing authorisation for a veterinary medicinal product where it appears, in particular following evaluation of the data referred to in article R. 5141-90, that the medicinal product no longer meets the conditions referred to in article L. 5141-6. In the…

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Article R5141-44 of the French Public Health Code

The decision to suspend, revoke or vary the marketing authorisation must state the reasons on which it is based and indicate the appeal procedures and deadlines. Except in cases of urgency, the decision may only be taken after the marketing authorisation holder has been invited to present his observations. When the authorisation is suspended, withdrawn or varied automatically, the marketing authorisation holder informs the stockholders so that they can take…

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Article R5141-45 of the French Public Health Code

Independently of decisions to suspend, modify or withdraw authorisations and as a precautionary measure, the Director General of the Agence nationale de sécurité sanitaire de l’alimentation, de l’environnement et du travail may prohibit the supply of certain batches of authorised veterinary medicinal products that are the subject of dispute and request the authorisation holder to recall these batches.

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Article R5141-47 of the French Public Health Code

Decisions to grant, automatically vary, refuse, renew or revoke marketing authorisations subject to the national procedure are taken in accordance with the procedures laid down in Article R. 5141-27 relating to the examination of these applications. They may only be the subject of a contentious appeal after an informal appeal has been lodged with the Director General of the Agency. Decisions to grant, automatically vary, suspend or revoke a marketing…

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Article R5141-47-1 of the French Public Health Code

In order to obtain a marketing authorisation for a medicinal product which is not covered by the marketing authorisation procedure issued by the European Commission pursuant to Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004, in more than one Member State of the European Union, the applicant must follow one of the two procedures provided for in this subsection: -either the mutual…

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Article R5141-47-2 of the French Public Health Code

In order to obtain recognition, by at least one other Member State of the European Union, of a marketing authorisation issued by the Director General of the Agence nationale de sécurité sanitaire de l’alimentation, de l’environnement et du travail, with France then acting as reference State, the holder of this authorisation asks the latter to update or prepare the assessment report for the veterinary medicinal product; he/she sends any additions…

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Article R5141-47-3 of the French Public Health Code

In order to obtain recognition in France of a marketing authorisation issued by another Member State of the European Union, known as the reference State, the holder of this authorisation must submit a marketing authorisation application to the Director General of the Agence nationale de sécurité sanitaire de l’alimentation, de l’environnement et du travail. From receipt of the assessment report on the medicinal product, accompanied by the summary of product…

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Article R5141-47-4 of the French Public Health Code

In order to obtain a marketing authorisation in France and in at least one other Member State of the European Union, for a veterinary medicinal product which does not have any authorisation in the European Union, the applicant sends an application for a marketing authorisation to the Director General of the Agence nationale de sécurité sanitaire de l’alimentation, de l’environnement et du travail. 1° If the applicant designates France as…

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Article R5141-47-5 of the French Public Health Code

In the event of agreement within the coordination group, referred to by the Director General of the Agence nationale de sécurité sanitaire de l’alimentation, de l’environnement et du travail or by another State : 1° In the case provided for in Article R. 5141-47-2, the Director General of the Agency notifies the States concerned and the holder of the agreement. In accordance with the assessment report thus approved, he will…

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