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Showing 741–750 of 37027 articles for “Art. L 623-32”
For medical devices to be subject to clinical investigations, the manufacturer must comply with the provisions of Title II of Book I of Part I of this Code.
In the case of external quality control, the return to conformity of the devices is certified by the compliant results of a second quality control carried out on the device in accordance with the prov…
Authorised bodies shall inform the Director General of the Agence nationale de sécurité du médicament et des produits de santé : 1° of any modification likely to alter the conditions under which autho…
The departments and bodies responsible for providing information are not obliged to comply with requests for information that are manifestly unreasonable in number or systematic in nature.
Without prejudice to the powers of the ethics officer provided for in article 28 bis of the aforementioned Act of 13 July 1983, employees involved in labour inspection activities may refer to the Cons…
I. - The hospitalisation sector of the paediatric critical care unit includes a minimum number of beds determined as follows: 1° At least eight beds for the paediatric critical care unit referred to i…
Where the Director General of the Regional Health Agency objects to the budget, he shall set a time limit, not exceeding thirty days from notification of the objection, within which the director of th…
Hospital practitioners are entitled to the reimbursement of expenses incurred in connection with their temporary travel for service purposes or, without prejudice to the provisions of article R. 6152-…
A staff representative who, during his/her term of office, no longer fulfils the conditions laid down in article R. 6152-322 for sitting on the section for which he/she was elected or has been dismiss…
Subject to the age limit extension rights applicable to them under the provisions of article 46 of law no. 87-588 of 30 July 1987 on various social measures, the age limit for practitioners governed b…
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