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Showing 7111–7120 of 60102 articles for “Art. Cass. 1ère civ. 5-1-2023 n° 21-13.966 FS-B”
Before examining the application for assessment, the approved body will ensure that the file includes in particular : - the general characteristics of the applicant, such as company name, name, addres…
The Director General of the Agence nationale de sécurité du médicament et des produits de santé shall decide on the application within seven months of the date of receipt of the complete file. Failing…
When the acquisition, possession and supply of veterinary medicinal products by the groups provided for in the first paragraph of article L. 5143-6 are carried out under the supervision of a pharmacis…
In each region, regional material vigilance and reactovigilance coordinators carry out their vigilance duties under the conditions defined in article R. 1413-61-4.
The Director General of the Agence nationale de sécurité du médicament et des produits de santé (French National Agency for the Safety of Medicines and Health Products) carries out his duties relating…
Members of commissions, committees, working groups and other expert collegiate bodies, as well as external experts used by the Agency and appearing on a list drawn up by the Agency's Director General,…
In order to safeguard the health and safety of the persons accommodated, the public and the staff, the Director General of the Regional Health Agency, when he is aware of facts which may be considered…
Patients who are offered temporary accommodation are given full information about the characteristics of the accommodation, in particular the financial contribution that they and any accompanying pers…
Upon medical assessment of the need to derogate from the maximum periods of non-medical accommodation provided for in article R. 6111-56, the limitations provided for in this article are not applicabl…
Persons accommodated under this section may share their room with one or more accompanying persons, subject to the accommodation facility's capacity.
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