Article R7345-15
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…
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Showing 6191–6200 of 28297 articles for “Art. Cass. 3e civ. 7-7-2016 n° 15-12370”
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…
Failure to comply with the provisions of article L. 7422-8 or the regulations made for their application is punishable by a fourth-class fine, imposed as many times as there are workers concerned.
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 declarations provided for in Article L. 5131-5 shall be made in accordance with the procedures and standard form laid down by order of the Minister for Health on a proposal from the Director Gener…
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 provisions of article R. 5211-21 are applicable to in vitro diagnostic medical devices.
Local reactovigilance correspondents are responsible for : 1° Recording and analysing any reported incident or risk of incident likely to be due to an in vitro diagnostic medical device; 2° Declaring…
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