Article D4362-18
…s the patient within the confines of the optician's shop or in a room adjoining it, designed to enable the patient to be cared for in conditions of sound and visual isolation and to ensure the confide…
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Showing 1361–1370 of 61134 articles for “Art. L 533-18-1”
…s the patient within the confines of the optician's shop or in a room adjoining it, designed to enable the patient to be cared for in conditions of sound and visual isolation and to ensure the confide…
The partnership is subject, where they exist, to the disciplinary provisions applicable to the profession. It may not be subject to disciplinary proceedings independently of those brought against one…
When the in-house pharmacy dispenses a blood-derived medicinal product directly to a patient, the information referred to in article R. 5121-187 is transcribed onto a special register marked and initi…
Dispensing pharmacists who dispense a blood-derived medicinal product must immediately transcribe the information mentioned in article R. 5132-10, the patient's date of birth and the information appea…
The provisions of article R. 6251-3 are applicable to the reports of the experts appointed by the consular chambers mentioned in article R. 6261-16. The reports are systematically sent to the educatio…
Bodies involved in activities designed to validate acquired experience keep separate accounts for this activity when they simultaneously carry out several other activities.
The court shall give its decision promptly in accordance with the ordinary oral procedure. The parties are not required to constitute a lawyer. The judgment is rendered in the first and last instance.…
For the application of Article R. 5127-13, where, due to the circumstances that led to the sample being taken or the appearance of the sample, as the case may be, the Director General of the Agence na…
Medical devices which comply with the standards applicable to them, transposing the harmonised European standards, the references of which have been published in the Journal officiel de la République…
For a new device, the Director General of the Agence nationale de sécurité du médicament et des produits de santé may, at any time and for a period of two years following the declaration provided for…
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