Article L6156-3
The rules defined for the presentation of medical, odontological and pharmaceutical staff of the public health establishments mentioned in Chapters I and II of this Title in professional elections are…
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Showing 5761–5770 of 46105 articles for “Art. I-f”
The rules defined for the presentation of medical, odontological and pharmaceutical staff of the public health establishments mentioned in Chapters I and II of this Title in professional elections are…
I. - The use of one of the persons mentioned in 2° of I, II and III of article R. 621-31 shall be governed by a memorandum of understanding signed with the Autorité des marchés financiers, which sets…
Breaches of articles L. 3232-5 and L. 3232-6 are recorded by the agents mentioned in article L. 511-3 and in 1° and 2° of I of article L. 511-22 of the French Consumer Code, under the conditions set o…
Article L. 430-2 is amended as follows:1° In the first paragraphs of I to III, the word "three" is replaced by the word "two";2° The last paragraphs of I to III are deleted;3° IV is repealed.
The establishments mentioned in the first paragraph of I shall publish the information provided for in II of article L. 312-19 and in the fourth paragraph of I of article L. 312-20 in their annual rep…
In accordance with the conditions laid down by decree of the Conseil d'Etat, the assets of an undertaking for collective real estate investment are made up of :1° At least 60% in property assets. In t…
I. - Companies producing or marketing products mentioned in 14°, 15° and 17° of article L. 5311-1 or providing services associated with these products shall make public, under the conditions defined i…
A medical file is created for each patient hospitalised in a public or private health establishment. This file contains at least the following elements, classified as follows : 1° Formalised informati…
The penalties for canvassing offences in the field of insurance are set out in the provisions of Chapter II of Title I of Book I of the Insurance Code.
For medical devices to be subject to clinical investigations, the manufacturer must comply with the provisions of Title II of Book I of Part I of this Code.
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