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Showing 2131–2140 of 68091 articles for “Art. s. L 233-3 and R 225-31”
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…
The marketing authorisation is granted by the Director General of the Agence nationale de sécurité du médicament et des produits de santé. The authorisation includes the national number identifying th…
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…
Establishments 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 neonato…
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…
Each year, the birthing centre 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.
The articles L. 2242-1 to L. 2242-4 are applicable to the communes of French Polynesia.
The agenda for Social and Economic Committee meetings is sent by the Chairman to the Committee members, to the Labour Inspectorate official referred to in Article L. 8112-1 and to the Social Security…
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