Article R5139-2
The authorisation referred to in article R. 5139-1 : 1° Operations relating to proprietary medicinal products for human use, proprietary medicinal products for veterinary use, experimental medicinal p…
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Showing 13561–13570 of 39711 articles for “Art. al. 3”
The authorisation referred to in article R. 5139-1 : 1° Operations relating to proprietary medicinal products for human use, proprietary medicinal products for veterinary use, experimental medicinal p…
The information mentioned in 1° to 3° of article R. 5138-1, with the exception of the name of the establishment's legal representatives, is entered in the European Union database.
…diseases and AIDS, in particular with a view to screening and, where appropriate, early treatment; 3° Discuss a regular contraception method that is appropriate for the patient.
When a minor has been dispensed the medicinal products indicated in the emergency contraception, the pharmacist sends the health insurance fund to which he belongs an invoice drawn up on a care sheet…
I. - The establishments or organisations mentioned in article L. 513-11-1 shall appoint a person responsible for the collection activity, who shall ensure compliance with the regulations relating to t…
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…
The declaration provided for in Article L. 513-10-2 shall be sent by any means giving a date certain to the Agence nationale de sécurité du médicament et des produits de santé. It shall indicate 1° Th…
…se containing micro-organisms or toxins are dispensed under the conditions set out in articles R. 5132-6 and R. 5132-7 and in the last two paragraphs of I of article R. 5141-112. The quantities dispen…
The loss or theft of micro-organisms or toxins as well as products containing them, any incident or accident as well as any event likely to result in their dissemination must be immediately declared t…
I. - Before issuing the authorisation applied for, the Director General of the Agence nationale de sécurité du médicament et des produits de santé (French National Agency for the Safety of Medicines a…
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