Article R4332-11
The following are set by order of the Minister for Higher Education and the Minister for Health:1° The composition of the file submitted in support of the application for authorisation;2° The composit…
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Showing 1861–1870 of 5900 articles for “Art. 494-11”
The following are set by order of the Minister for Higher Education and the Minister for Health:1° The composition of the file submitted in support of the application for authorisation;2° The composit…
The commission examines the knowledge, skills and competencies acquired during the person's initial training, professional experience and lifelong learning which have been validated by a competent bod…
The information referred to in article R. 4354-10 is transmitted when the training qualification is obtained.
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.-…
Private individuals may only import a medicinal product in a quantity compatible with personal therapeutic use for a period of treatment not exceeding three months under normal conditions of use, or f…
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…
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