Article R5132-42-3
…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…
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Showing 8491–8500 of 35538 articles for “Art. Cass. 1re civ. – 4 Apr. 2024 – no. 21-22.949”
…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…
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…
…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'al…
…of forty-five days from the date of receipt of the complete application referred to in Article R. 5141-123-3. The period mentioned in the previous paragraph is reduced to twenty days if the applicatio…
For each batch of medicinal products referred to in articles R. 5142-45 and R. 5142-46, the pharmacist or veterinarian responsible shall release the batches and certify that each manufacturing batch c…
Pharmaceutical establishments carrying out one or more of the operations making up the operation must have a documentation system comprising the procedures and records covering the operations they car…
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