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Showing 9661–9670 of 64357 articles for “Art. R 418-6 and R 418-7”
Care is organised in such a way that, depending on the patient's clinical condition, at least two sequences of treatment, including at least one individual treatment, are provided each working day in…
In addition to the teams provided for in article D. 6124-177-3, the multidisciplinary team includes: 1° At least one masseur-physiotherapist; 2° At least one psychologist; 3° At least one young child…
The coordinating doctor specialises in paediatrics and in this case has proven training or experience in rehabilitation, or specialises in physical and rehabilitation medicine and in this case has pro…
I. - The trade union(s) requesting the organisation of the consultation shall notify the employer and the other representative trade union(s) of their request in writing within one month of the date o…
The maximum amount of aid is €9,378.
In the case of active implantable medical devices or medical devices in Class III or Class II b, the manufacturer shall take all necessary measures to ensure that the manufacturing process guarantees…
As part of the EC verification procedure, the manufacturer submits the devices manufactured for inspection by an authorised body. The authorised body checks the conformity of the medical devices with…
For Class IIa medical devices or Class I medical devices, the provisions of Article R. 5211-43 apply subject to the following modifications: 1° For class II a medical devices, the authorised body veri…
The offences which may give rise to the issue of a European arrest warrant are, under the law of the issuing Member State, the following: 1° Offences punishable by deprivation of liberty for a period…
The European arrest warrant sent to the competent authority of another Member State must be translated into the official language or one of the official languages of the executing Member State or into…
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