Article D6124-177-53
…premises provided for in article D. 6124-177-1, the authorised site includes a communal living area and spaces allowing the patient's family and friends to participate.
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Showing 5861–5870 of 59015 articles for “Art. 10 and 11”
…premises provided for in article D. 6124-177-1, the authorised site includes a communal living area and spaces allowing the patient's family and friends to participate.
Depending on the patient's clinical condition, the authorisation holder offers each patient treatment in at least two of the following therapeutic practices: -psychological care; -therapeutic educatio…
In addition to the teams provided for in article D. 6124-177-3, the multidisciplinary team includes at least one psychologist. The members of the multidisciplinary team must have proven training or ex…
…a patient is admitted on a part-time basis. Whenever necessary, on the basis of a medical proposal and with the patient's agreement, they may involve one or more members of the patient's family.
…on granted by the European Union pursuant to Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004 laying down Community procedures for the authorisation and super…
The information provided for in Articles R. 5121-138 and R. 5121-139 is written in French. They may also be written in other languages, provided that the same information appears in all the languages…
…tion No 2016/161 EU of 2 October 2015 supplementing Directive 2001/83/EC of the European Parliament and of the Council by laying down detailed rules concerning safety features on the packaging of medi…
…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") and, where…
…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, where the…
…tion No 2016/161 EU of 2 October 2015 supplementing Directive 2001/83/EC of the European Parliament and of the Council by laying down detailed rules concerning safety features on the packaging of medi…
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