Article R4362-11
The issue of corrective ocular contact lenses by a spectacle optician to a person wearing them for the first time is subject to the presentation of a medical or orthoptic prescription stating the corr…
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Showing 2171–2180 of 38648 articles for “Art. L 441-11”
The issue of corrective ocular contact lenses by a spectacle optician to a person wearing them for the first time is subject to the presentation of a medical or orthoptic prescription stating the corr…
The following are laid down by order of the Minister for Health:1° The composition of the file submitted in support of the application for authorisation ;2° The composition of the aptitude test panel…
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…
The standards and methods applicable to the testing of medicinal products are set, on a proposal from the Director General of the Agence nationale de sécurité du médicament et des produits de santé, b…
I.-Articles R. 4233-33 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.-…
Except where there are public health reasons for not doing so, parallel import authorisation is granted if the following conditions are met: 1° The proprietary medicinal product is obtained from an au…
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…
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…
If the Director General of the Agence nationale de sécurité du médicament et des produits de santé remains silent, the authorisation will be refused on expiry of a period of forty-five days from the d…
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