Article L954-3-3
Article L. 441-9 is amended as follows:1° In the second paragraph, the words "within the meaning of 3 of I of l'article 289 du code général des impôts," are deleted;2° In the fourth paragraph , the wo…
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Showing 5441–5450 of 69694 articles for “Art. L 144-2 and Art. R 132-5-3”
Article L. 441-9 is amended as follows:1° In the second paragraph, the words "within the meaning of 3 of I of l'article 289 du code général des impôts," are deleted;2° In the fourth paragraph , the wo…
Practitioners placed on compulsory lay-off pursuant to the fifth paragraph of article L. 6152-5-2 may benefit from the insurance allowance provided for in article L. 5424-1 of the Labour Code under th…
An employer who contests the nature, extent or time limit imposed by the Labour Inspectorate inspecting officer on a request for product analysis made pursuant to Article R. 4722-29, shall submit his…
Unless there are provisions to the contrary, confirmed by the founding decision, the union's membership of a public establishment for inter-municipal cooperation is subject to the agreement of the mun…
A tattooing product may only be placed on the market, whether free of charge or for a fee, if it meets the following conditions: 1° Its container and packaging must bear the name or company name and a…
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…
The procedures for issuing communication permits to lawyers and the rules applicable to relations between detainees and their defence counsel are determined by the provisions of articles R. 313-14, R.…
By way of derogation from the provisions of the first sub-section, the provisions of this sub-section apply to the manufacture and importation of investigational medicinal products.
For investigational medicinal products, the documents relating to each batch are kept by the pharmaceutical establishment which manufactures it, for at least five years after the end of the trial or t…
The importing pharmaceutical establishment shall ensure that the investigational medicinal products it imports have been subjected to standards of good manufacturing practice at least equivalent to th…
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