Article D4383-1
The scale of assistance referred to in article L. 4383-4 granted in the form of study grants comprises, on the one hand, levels to which minimum income ceilings correspond and, on the other hand, a li…
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Showing 6551–6560 of 53704 articles for “Art. CA Paris 1-12-2021 n° 20/04742”
The scale of assistance referred to in article L. 4383-4 granted in the form of study grants comprises, on the one hand, levels to which minimum income ceilings correspond and, on the other hand, a li…
…oducts for adults and children; 4° Information which may be useful to the pharmacist for pharmaceutical practice. The pharmacopoeia indicates the characteristics of medicinal products, the means by wh…
…o medicinal products for human use, as well as the particulars relating to authenticity and identification, including the national number identifying the presentation of the medicinal product referred…
…counted from the date of issue of the registration. For registrations issued up to the date of publication of decree no. 2008-436 of 6 May 2008 relating to the registration of homeopathic medicinal pr…
…marketing authorisation in France, the Director General of the Agence nationale de sécurité du médicament et des produits de santé may, subject to the measures he deems necessary to protect human hea…
I. - The applicant or the holder of the registration shall forward to the Agency without delay, indicating the scope of the information, any new information which it has or becomes aware of after the…
…ollowing information: 1° The name of the medicinal product or product, the strength, the pharmaceutical form and, where appropriate, a reference to the recipient ("infants", "children" or "adults") an…
…ter registration, manufacturing methods and control techniques take account of scientific and technical progress. Any resulting changes must first be registered under the conditions set out in article…
…ollowing information: 1° The name of the medicinal product or product, the strength, the pharmaceutical form and, where appropriate, the name of the recipient ("infants", "children" or "adults") and,…
…ons and for the reasons that justify them, the Director General of the Agency may prohibit, as a precautionary measure, the supply of a registered medicinal product, limiting this prohibition, where a…
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