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Showing 2791–2800 of 26757 articles for “Art. Aut. conc. n° 11-DCC-214 du 29 Dec 2011”
The information referred to in article R. 4354-10 is transmitted when the training qualification is obtained.
…ical or orthoptic prescription stating the correction and the essential characteristics of these products, the list of which is set by order of the Minister for Health.These prescriptions are valid fo…
…rt of the application for authorisation ;2° The composition of the aptitude test panel and the procedures for organising this test;3° The terms and conditions under which an adaptation period, an apti…
At least thirty days before the date of the election, candidates shall hand in their signed declaration of candidacy to the head office of the Association's body, in return for a receipt, or send it t…
…233-33 to R. 4233-38 are applicable in New Caledonia and French Polynesia in the version set out in Decree no. 2022-381 of 16 March 2022, subject to the adaptations set out in II. II.- For application…
The proprietary medicinal product for which parallel import authorisation is sought may differ from the proprietary medicinal product which has already obtained marketing authorisation in France, as r…
The package leaflet of the proprietary medicinal product benefiting from a parallel import authorisation is identical to that of the proprietary medicinal product which has obtained marketing authoris…
…le L. 4211-9; 2° The country of origin and, if different, the country of origin of the medicinal product; 3° Its name, composition, pharmaceutical form, strength and route of administration; 4° The qu…
The labelling and outer packaging of the proprietary medicinal product benefiting from a parallel import authorisation are identical to those of the proprietary medicinal product which has obtained ma…
…R. 5125-8, alterations to the building, or related to the implementation of a new activity, must be declared in advance to the general director of the regional health agency and to the competent counc…
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