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Showing 1991–2000 of 63870 articles for “Art. L 3332-14 and L 3332-26”
The free and informed consent of the person being examined or cared for is sought in all cases. If the patient, in a condition to express his/her wishes, refuses the proposed treatment, the nurse shal…
I.-The labelling of the medicinal products mentioned in 1° of II of article L. 5121-12 includes at least the following information: 1° The name of the medicinal product or, where appropriate, its code…
The automatic processing of personal data relating to breaches of the provisions of the general terms and conditions of sale or the internal regulations concerning safety, which may be implemented by…
An inter-institutional cluster, as provided for in 3° of II of article L. 6147-16, is set up under the conditions specified by the agreement provided for in this article in order to implement the part…
A partial internal model shall be approved by the Autorité de contrôle prudentiel et de résolution only where it meets the requirements set out in Article R. 352-13 and the following conditions: a) It…
Before 31 March each year, each medical biology laboratory shall declare electronically to the regional health agency within whose jurisdiction it is established, the total number of medical biology e…
Each year, the mediator referred to in article L. 5315-4 submits a report to the institution's Board of Directors, in which he or she makes any proposals he or she feels are likely to improve the oper…
Beneficiaries are obliged to inform us immediately of any change in their situation with regard to the amount of income they receive.
Any professional legally established in another Member State of the European Union or party to the Agreement on the European Economic Area who engages, on a temporary and occasional basis, in the prac…
The liquidator referred to in article R. 427-13 of this Code shall, with the agreement of the Fund, manage the files relating to compensation for damage covered by insurance, the subscription of which…
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