Article R5121-35
The Director General of the Agence nationale de sécurité du médicament et des produits de santé will make a decision within two hundred and ten days of the submission of a complete application file. W…
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Showing 7491–7500 of 64513 articles for “Art. L. 133-4 et R. 133-3”
The Director General of the Agence nationale de sécurité du médicament et des produits de santé will make a decision within two hundred and ten days of the submission of a complete application file. W…
After the marketing authorisation has been granted, the authorisation holder must, with regard to the manufacturing and control methods, take account of scientific and technical progress and introduce…
For public health reasons, the Agence nationale de sécurité du médicament et des produits de santé may require a company to submit samples of each batch of the bulk product and the finished product fo…
I.- Veterinary proprietary medicinal products and auto-vaccines for veterinary use containing micro-organisms or toxins are prescribed under the conditions mentioned in I, III and IV of article R. 514…
Persons authorised to supply proprietary medicinal products for human use, proprietary veterinary medicinal products, investigational medicinal products for human use or auto-vaccines for veterinary u…
…ments providing care for pregnant women and newborn babies include, on the same site, either an obstetrics unit, or an obstetrics unit and a neonatology unit, or an obstetrics unit, a neonatology unit…
The application for authorisation referred to in Article L. 6323-4-3 shall be sent to the Director General of the Regional Health Agency by any means that provides a date of receipt. It is accompanied…
…entre draws up and sends to the regional health agency an activity report, the content of which is set by order of the Minister for Health.
Tangible pledge loans taken out with municipal credit unions pursuant to Article L. 514-1 of the Monetary and Financial Code are subject to the provisions of articles L. 312-5, L. 312-6 and L. 312-8 t…
The Competition Authority may sit either in plenary session, in sections or as a standing committee. The standing committee is made up of the chairman and four vice-chairmen.The authority's panels del…
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