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Showing 6351–6360 of 30762 articles for “Art. Cass. 3e civ. 28-5-2003 n° 676”
The compassionate prescribing framework drawn up by the Director General of the Agence nationale de sécurité du médicament et des produits de santé states in particular, for each medicinal product: 1°…
Before removing or partially or totally covering the safety features provided for in article R. 5121-138-2, the pharmaceutical establishment which manufactures medicinal products shall check that the…
By way of derogation from the provisions of the first sub-section, the provisions of this sub-section apply to the manufacture and importation of investigational medicinal products.
For investigational medicinal products, the documents relating to each batch are kept by the pharmaceutical establishment which manufactures it, for at least five years after the end of the trial or t…
The manufacturer or importer of investigational medicinal products shall ensure that all manufacturing operations are carried out in accordance with the information provided by the sponsor in the appl…
For each representative, an alternate is appointed under the same conditions as the full member. Alternates may attend meetings of the Regional Employment, Training and Vocational Guidance Committee w…
When the funding from the allocation mentioned in I of article D. 6123-26-1 is not sufficient to cover a request for a professional transition project, the regional interprofessional joint committee m…
Regional cross-industry joint committees cannot be designated as operators of professional development advice by France Compétences.
Persons who complete a vocational training course for which the prison administration is responsible outside the institution under a semi-liberty or work release scheme are entitled to the remuneratio…
Subsection 4 of Section 4 of Chapter I of Title III of Book III of this Part shall not apply to Mayotte.
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