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Showing 2411–2420 of 37961 articles for “Art. L 441-17”
I. - For the persons mentioned in 1° to 6° and 7° bis of Article L. 561-2, the obligations laid down in I and III of Article L. 561-5 and in Article L. 561-5-1 may be implemented by a third party in e…
I.-The Autorité des marchés financiers shall consist of a Board, an Enforcement Committee and, where applicable, specialised commissions and consultative committees. Unless otherwise provided, the pow…
The company which exploits a proprietary medicinal product contributes to its proper use by ensuring in particular that the product is prescribed in compliance with its marketing authorisation referre…
The enforcement measures provided for in Article L. 412-1 : 1° Les dispositions des articles 1er, 2, des paragraphes 1 à 3, de l'article 9, de l'article 10, de l'article 11 des paragraphes 1 et 2 de l…
I.-The holder of a "B" nuclear medicine authorisation pursuant to Article R. 6123-135 has an in-house pharmacy authorised to carry out the activity provided for in 6° of Article R. 5126-9 and, where a…
The role of the radiopharmacist provided for in article D. 6124-189 is to ensure the safety of the radiopharmaceutical medicine circuit and includes in particular: 1° Carrying out control actions rela…
I.-The holder of the "A" authorisation pursuant to Article R. 6123-135 shall have a team comprising: 1° At least one doctor specialising in nuclear medicine present on site during patient care; 2° At…
The equipment on the site authorised under the conditions of Article R. 6123-136 is connected to a system for archiving and sharing images and to a system for archiving and analysing doses. The report…
The authorised nuclear medicine site has the following equipment: 1° An emergency trolley for the treatment of patients requiring it; 2° Equipment for waste and effluent management in accordance with…
The authorisation holder is subject to the obligation of quality assurance defined in I of Article L. 1333-19.
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