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Showing 3351–3360 of 8385 articles for “Art. CE 26-11-1982 n° 30956”
The safety features may only be replaced by equivalent safety features in order to verify the authenticity, identify and provide proof of unlawful handling of the medicinal product. This replacement i…
…ictogram, the model of which is determined, after consultation with the Director General of the Agence nationale de sécurité du médicament et des produits de santé, by order of the Minister for Health…
Without prejudice to the provisions of Article R. 5132-15, the labelling of the immediate packaging and, if available, the outer packaging of the preparations mentioned in 1° to 3° of Article L. 5121-…
…of 2° of the same article, as well as : 1° Where the preparation contains up to three active substances, the common name or names ; 2° The route of administration if the product is intended to be admi…
For the classification and allocation of aid in year n, the reference period runs from film week 27 of year n-3 to film week 26 of year n-1. In the cases mentioned in…
For medicinal products containing radionuclides, in addition to the information provided for in article R. 5121-140, the labelling of the protective shielding provides all the explanations relating to…
Where proceedings are pending before the industrial tribunal on the date of the judgment opening the receivership, the information relating to the subject matter and circumstances of the dispute and t…
Articles R. 625-1 to R. 625-7 are applicable to receivership proceedings.
Any person who sterilizes with a view to placing on the market CE-marked medical devices designed by their manufacturer to be sterilized before use or systems or kits referred to in Section 10 of this…
When advertising in favour of a veterinary pharmaceutical company or establishment mentions a veterinary medicinal product, it is governed by the provisions of Section 8 of Chapter I of this Title. Th…
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