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Showing 5741–5750 of 36396 articles for “Art. Décret n° 2015-1437 du 5 novembre 2015”
Where batches of investigational medicinal products come from another Member State of the European Community or party to the Agreement on the European Economic Area and are manufactured or imported in…
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…
…isions 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…
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…
…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 any medicinal product that may give rise to a conditional dispensing prescription as referred to in article L. 5121-12-1-1, and without prejudice to the information provided for in article R. 5132…
…er of units appearing in an initial outer packaging that complies with the provisions of article R. 5121-138, when the pharmacist dispenses the last units appearing therein, they are, by way of deroga…
Persons providing information by canvassing or prospecting for veterinary medicinal products, including medicated feedingstuffs, must meet one of the following qualification requirements: 1° Hold one…
Notwithstanding the provisions of Article R. 5222-18-4, where the second-hand in vitro diagnostic medical device which is the subject of the transfer has never been put into service, the file consists…
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