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Showing 4241–4250 of 26223 articles for “Art. 477 to 494”
Establishments or authorised organisations shall draw up and keep up-to-date a full list of the agreements they have entered into with third parties whose involvement has an influence on the quality a…
…pared on an ad hoc basis are distributed, under the responsibility of the person in charge referred to in article R. 4211-37 or, where applicable, the person in charge of site activities referred to i…
An authorised establishment or organisation may transfer to another authorised establishment or organisation advanced therapy medicinal products prepared on an ad hoc basis with a view to their storag…
Changes other than those mentioned in articles R. 4211-43 and R. 4211-44 are declared in the annual activity report provided for in article R. 4211-47.
In the event of non-compliance with the legislative and regulatory provisions or the conditions of the authorisation, the suspension, which may not exceed one year, and the withdrawal of the authorisa…
The authorised establishment or body sends the Director General of the Agence nationale de sécurité du médicament et des produits de santé and the Director General of the Agence de la biomédecine, as…
I. - Environmental assessment tabulated by the debtorName of the operator:Company name: Name of the insolvency administrator: 1. Identification of the site City: Department: Usual designation of the s…
…five members. It is made up of representatives of: 1° Public administrations; 2° Producers; 3° Operators; 4° Users. The representatives in the first category are appointed by the prefect responsible f…
…of the file, with the exception of the document mentioned in 2° of article A. 761-11. He indicates to the manager the deadline by which the latter must inform him of the availability or otherwise of…
…personal assets and of the beneficiary of the waiver 1. Identity of the sole trader Birth name: Customary name, if any: Forenames (in order of civil status): Nationality: Born on I _ I _ I _ I _ I _…
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