Article R7111-15
After examination, and under the conditions set out in articles R. 7111-27 and R. 7111-28, the Professional Journalist Identity Card Commission decides on applications for the issue of honorary profes…
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Showing 2481–2490 of 33178 articles for “Art. Cass. com. 24-5-2016 n° 15-17.788”
After examination, and under the conditions set out in articles R. 7111-27 and R. 7111-28, the Professional Journalist Identity Card Commission decides on applications for the issue of honorary profes…
The single, simplified declaration concerns the recruitment and employment of performing artists as well as workers and technicians in the performing arts occupying one of the jobs defined by the agre…
The decision to withdraw authorisation is published in the prefecture's registry of administrative acts. The prefect will inform the president of the departmental councils concerned, the minister resp…
I.-The role of the Platform Players' Council is to make proposals to the Chairman of the Board of Directors on matters falling within the remit of the establishment, in particular: 1° The working and…
The national monitoring, support and control group carries out or provides support for operations requiring special expertise, assistance for departments, specific control or coordination of controls.…
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…
For the purposes of this chapter, "establishment" means any place or site where one or more operations involving micro-organisms and toxins or products containing them are carried out.
The application for marketing authorisation is accompanied by a draft summary of product characteristics, the presentation and content of which are laid down in accordance with Article 14 of Directive…
The affixing of marks or inscriptions on a medical device, on its packaging or on the instructions for use which are likely to mislead as to the meaning or form of the CE marking is prohibited. Any ot…
The following incidents may be reported: 1° A noxious and unintended reaction occurring during the use of a medical device in accordance with its intended purpose; 2° A noxious and unintended reaction…
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