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Showing 3181–3190 of 39734 articles for “Art. L 132-9”
For the purposes of this Title, accessories to medical devices are treated as devices in their own right. Accessories are classified as such, independently of the devices with which they are used, wit…
If one or more of the bodies mentioned in article D. 5143-8, consulted with a view to setting up the Commission, have not formulated a proposal within one month of receiving the request from the Regio…
In vitro diagnostic medical devices appearing on the list established by the order referred to in Article R. 5221-6, designed and manufactured in accordance with common technical specifications publis…
Any project to modify the elements mentioned in 1° and 2° of article R. 5213-5 is the subject of a new authorisation application submitted and examined under the same conditions as the initial authori…
The Chairman sets the agenda on a proposal from the Chief Executive. Items which the Minister for Health, the Chairman of the Board of Directors or at least one third of its members request to be incl…
Service providers and equipment distributors update their professional knowledge and keep abreast of developments in best practice, legislation and regulations.
Any project to modify the elements mentioned in 1° and 2° of article R. 5223-5 is the subject of a new application for authorisation submitted and examined under the same conditions as the initial app…
The competent bodies of the health care organisation define, after consultation with the medical commission or conference, the procedures for implementing the collection, processing, validation and in…
A summary of the healthcare establishment's annual infection control programme is given to each patient with the welcome booklet.
A health establishment whose emergency medicine activity is below a threshold set by order of the Minister for Health may be authorised to carry out the activity mentioned in 3° of article R. 6123-1,…
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