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Showing 4601–4610 of 18481 articles for “Art. CE 5-5-2010 n° 301419”
…ng to these batches held by the manufacturing establishment located in the Member State or party concerned, which holds a manufacturing or import authorisation for such medicinal products or products…
The pharmaceutical establishment manufacturing medicinal products mentioned in 1° of article L. 4211-1, generators, kits or precursors mentioned in 3° of this article has a documentation system compri…
…may result in a risk to public health, he shall immediately notify the Director General of the Agence nationale de sécurité du médicament et des produits de santé.
…ioned in 4° of article L. 5121-1. The obligations laid down by these articles are applied by reference to the pharmacopoeia monographs which describe them.
…quired. The Director General of the Regional Health Agency registers the application and issues a receipt. It is examined under the conditions set out in articles R. 5125-2 to R. 5125-4.
The medicinal products, products or articles mentioned in article L. 4211-1 are transported by the pharmacist dispensing them at home under conditions which guarantee their perfect preservation.
…to 3° of article L. 5121-1, the name and address of the pharmacist who dispensed the preparation, except for ampoules and other small primary packaging mentioned in article R. 5121-146-3, for which on…
…is its name within the meaning of article R. 5121-1. He shall enter on the prescription the pharmaceutical form of the medicinal product dispensed if this differs from that of the medicinal product…
The holder of evidence of formal qualifications as a pharmacist issued by a Member State of the European Union or another State party to the Agreement on the European Economic Area who: 1° On 1 June 2…
The medicines, products or objects mentioned in article L. 4211-1 may only be dispensed at home in application of article L. 5125-25 when the patient is unable to travel, in particular due to their st…
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