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Showing 1881–1890 of 69143 articles for “Art. L 227-9-1 and D 227-1”
In the event that the service provider or equipment distributor is unable to provide the equipment or service adapted to the person who is ill or has an incapacity or disability, they will immediately…
Where they exist, the service provider and equipment distributor comply with the equipment prescription and recommendation issued by the multidisciplinary team under the conditions provided for in art…
In order to provide the most appropriate equipment for the needs of the person who is ill or has an incapacity or disability, the service provider and the equipment distributor will ask the prescriber…
The service provider and equipment distributor apply the advice on use and safety given by the equipment manufacturer. They provide the person who is ill or has an incapacity or disability and their f…
The head of the medical biology laboratory holding the authorisation is required to declare without delay to the Minister responsible for health any change relating to the legal rules and technical op…
The Minister for Health shall maintain and make available to the public a register of medical biology laboratories established in another Member State of the European Union or party to the Agreement o…
The competent authorities of the State in which the laboratory has its registered office are informed of the decision of the Minister for Health.
Renewal applications follow the same procedure as initial applications.
I.-The application for authorisation provided for in 3° of Article L. 6221-4 shall be sent by the medical biology laboratory established in another Member State of the European Union or party to the A…
The authorisation is issued for a period of five years. It specifies the medical biology tests or families of medical biology tests that the laboratory is authorised to perform at the request of a med…
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