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Showing 9721–9730 of 63349 articles for “Art. 3-2° to 4°”
The Minister for Health may, on a proposal from the Director General of the National Agency for the Safety of Medicines and Health Products, require by order that companies exploiting certain immunolo…
During the examination of marketing authorisation applications, the Director General of the Agence nationale de sécurité du médicament et des produits de santé may order any investigative measure he d…
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…
…sons, 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 for its inspection befo…
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…
…wborn 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 and a neonatal intensive care 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…
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.
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