Article R5132-42-1
The specific arrangements for packaging, labelling and information for the insured party, as well as traceability for medicinal products dispensed individually in dispensing pharmacies, are set out in…
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Showing 7271–7280 of 24307 articles for “Art. 4 janv. 2023”
The specific arrangements for packaging, labelling and information for the insured party, as well as traceability for medicinal products dispensed individually in dispensing pharmacies, are set out in…
The list drawn up by the order provided for in article L. 5123-8 of medicinal products which may be dispensed by the unit is established by reference to the medicinal product or the pharmaco-therapeut…
…in the form of a blister pack containing at least the information provided for in Article R. 5121-141, in outer packaging that complies with the provisions of Article R. 5121-138 ; 2° Or the medicina…
…ied out by the pharmacist either on renewal of the prescription by the nurse pursuant to article L. 4311-1, or on his own initiative under this article, or cumulatively by both, may not exceed a total…
The pharmacist must inform the woman concerned that this method of dispensing is non-renewable beyond 6 months and that she should consult a doctor or midwife if she intends to continue taking medicat…
The following are laid down by order of the Minister for Health, on a proposal from the Director General of the Agence nationale de sécurité du médicament et des produits de santé: 1° The list of subs…
…ing 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 t…
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 author…
The Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail or the applicant for marketing authorisation may refer the matter to the European…
…at the veterinary medicinal product in question falls within the categories defined in Article L. 5142-5-1, he will inform the reference State and the other States concerned that he is no longer takin…
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