Article L3131-10-1
I.- In the event of an exceptional health situation, the consequences of which exceed the capacity of one or more health care structures in the region, the Director General of the regional health agen…
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Showing 3881–3890 of 69879 articles for “Art. I-1°-a”
I.- In the event of an exceptional health situation, the consequences of which exceed the capacity of one or more health care structures in the region, the Director General of the regional health agen…
The Minister for Health or, by delegation, the Director General of the Centre National de Gestion may, following the opinion of a commission composed in particular of professionals, individually autho…
Persons engaged in the activity of brokering medicinal products as referred to in article L. 5124-19 are not subject to the provisions of this Title.
For the application of article L. 4113-14 to Wallis and Futuna, the words: "the representative of the State in the department" are replaced by the words: "the representative of the State in the territ…
The transfer to the commune of the property, rights and obligations of a section of communes is pronounced by the representative of the State in the département at the request of the municipal council…
I.-The département draws up a departmental plan for territorial solidarity within its territory. This plan defines, for a period of six years, a programme of actions designed to enable, in the departm…
Prior to the debates on the draft budget, the President of the Regional Council shall present a report on the situation with regard to equality between women and men concerning the operation of the re…
For the application of article L. 4132-5, the words: "and L. 145-2-1 of the Social Security Code" are replaced by the words: "and sentences handed down by the courts responsible for disputes relating…
The following definitions apply 1° "Investigational medicinal product" means a medicinal product which has been tested or used as a reference, including as a placebo, in a clinical trial; 2° "Authoris…
A generic medicinal product may not be marketed until ten years have elapsed following the initial marketing authorisation of the reference medicinal product. However, this period is extended to eleve…
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