Article R5127-19
The products seized are placed under seal and sent to the public prosecutor at the same time as the official report. If it is not possible to send them immediately, they are left with the person conce…
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Showing 7801–7810 of 24255 articles for “Art. L110-4”
The products seized are placed under seal and sent to the public prosecutor at the same time as the official report. If it is not possible to send them immediately, they are left with the person conce…
The provisions of 1° of article R. 5132-15 do not apply to the medicinal products mentioned in 2° and 3° of article R. 5124-43. However, the words: "Reserved for professional use", surrounded by a col…
List I medicinal products are kept in locked cabinets or premises containing nothing else, with the exception of dangerous substances classified as very toxic or toxic, in application of article L. 51…
The outer packaging of medicinal products covered by this section shall include : 1° If the medicinal product is intended for humans, a white space, surrounded by a coloured line, in which the dispens…
It is prohibited to use, for the medicinal products mentioned in article R. 5132-1, containers or packaging bearing the name of a product intended for human or animal consumption or likely to create c…
The authorisation holder shall carry out the assessment referred to in Article L. 6122-5, in accordance with the conditions laid down in this section.The purpose of this evaluation is to check that th…
The following health care activities are subject to the authorisation provided for in Article L. 6122-1, including when they are carried out in the form of alternatives to hospitalisation:1° Medicine…
The heavy equipment listed below is subject to the authorisation provided for in Article L. 6122-1:1° (Repealed) ;2° The following cross-sectional imaging equipment, with the exception of that exclusi…
The quantitative assessment of healthcare provision provided for in the fifth paragraph of Article L. 6122-9 is drawn up by the Director General of the Regional Health Agency and published at least fi…
In the event of a transfer of authorisation, including when this transfer is the result of a merger, the transferee must send the General Director of the Regional Health Agency a request for confirmat…
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