Article L6211-22
…Minister for Health, issued after consultation with the committee referred to in article L. 6213-12 and the Director General of the Agence nationale de sécurité du médicament et des produits de santé.
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Showing 361–370 of 56971 articles for “Art. 22-21.272 and 22-24.502”
…Minister for Health, issued after consultation with the committee referred to in article L. 6213-12 and the Director General of the Agence nationale de sécurité du médicament et des produits de santé.
The dimensions of workplaces, in particular their height and surface area, are such as to enable workers to perform their tasks without risk to their health, safety or well-being. The free space at th…
…of the list of members by the Board of Directors, from among persons recognised for their knowledge and skills in the field of ethics and professional conduct, and after examination of their links of…
Joint decrees by the Ministers of Labour and Agriculture set: 1° The methods for measuring concentration, flow rate, capture, filtration and purification efficiency; 2° The nature and frequency of ins…
…s, in particular the financial resources, that the project owner makes available to the coordinator and the authority it confers on the coordinator in relation to all those involved in the operation,…
The reciprocal rights and obligations of the inter-company occupational health and prevention service and its members are set out in its articles of association or internal regulations. These statutes…
…ion 1 of this section, with the exception of article R. 6523-19, are applicable to Saint-Barthélemy and Saint-Martin subject to the following adaptations:1° The powers of the Regional Committee for Em…
…They are elected by secret ballot in a two-round list system, based on proportional representation and the highest average, with preferential voting and without a mixture of votes. Lists may include…
In order to comply with the essential requirements relating to design and manufacture, medical devices, other than active implantable devices, must be designed, manufactured and packaged in such a way…
…rt of an incident or risk of incident caused by medical devices used in the collection, manufacture and administration of blood-derived products;2° Informing the manufacturers concerned of the inciden…
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