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Article R5213-5 of the French Public Health Code

The application for authorisation to advertise the medical devices referred to in Article L. 5213-4 shall be sent to the Director General of the Agence nationale de sécurité du médicament et des produits de santé by the person for whose benefit the advertising is to be disseminated, by registered letter or by electronic means with acknowledgement of receipt or delivered against receipt. Each application for authorisation must be accompanied by…

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Article R5213-7 of the French Public Health Code

The Director General of the Agence nationale de sécurité du médicament et des produits de santé will notify the applicant of his decision on prior authorisation within two months of the date of receipt of the complete dossier. Authorisation is deemed to have been granted in the absence of a decision by the Director General of the Agency within this period. If the applicant’s documents are not complete, the Agence…

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Article R5213-9 of the French Public Health Code

Any project to modify the elements mentioned in 1° and 2° of article R. 5213-5 is the subject of a new authorisation application submitted and examined under the same conditions as the initial authorisation application. This authorisation continues to run until its initial expiry date.

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Article R5213-10 of the French Public Health Code

Authorisation may be suspended or withdrawn by reasoned decision of the Director General of the Agence nationale de sécurité du médicament et des produits de santé where the advertising of the medical device no longer complies with the conditions laid down by the provisions of Articles L. 5213-2 and L. 5213-4, and by the provisions of this chapter. Suspension or withdrawal may only take place after the holder has been…

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