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Showing 5641–5650 of 17987 articles for “Art. 5 avr. 1978”
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.
…blishments importing investigational medicinal products under the conditions set out in articles R. 5124-57-3 and R. 5124-57-4 hold these documents and keep them for the same period of time. When the…
I.-In application of 7° of article L. 5125-1-1 A, the patient may designate a pharmacist who holds a dispensary or who manages a mutualist or miner's aid pharmacy, participating in the same coordinate…
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…
…1 and, where applicable, the decision of the competent professional body referred to in article R. 5125-24-4. On receipt of this document, the Registrar will register the company and inform the Presi…
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…
A statutory auditor shall certify the annual accounts of the fund referred to in the second paragraph of II of Article L. 6131-4.
…the third paragraph of article L. 6323-17-1, mobilise the allocation mentioned in article R. 6123-25 to provide additional funding.
Regional cross-industry joint committees cannot be designated as operators of professional development advice by France Compétences.
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