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Showing 5531–5540 of 8507 articles for “Art. 1594 D”
When a medical biology laboratory established in another Member State of the European Union or party to the Agreement on the European Economic Area carries out the analytical phase of medical biology…
Applications for authorisation may only be examined if they are accompanied by a complete file. The application is deemed to be complete if, within one month of receipt, the Minister for Health has no…
The application for authorisation provided for in the third paragraph of Article L. 6211-2-1, as it read prior to the entry into force of amended Order No 2010-49 of 13 January 2010 relating to medica…
Where it is established that the operating conditions of the laboratory holding the authorisation are not or are no longer equivalent to those imposed, under the first paragraph of Article 7 of Order…
The head of the 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 operating standard…
The competent authorities of the State in which the laboratory has its registered office are informed of the decision of the Minister for Health.
The application for authorisation must be accompanied, where appropriate, by a copy of the documents representing authorisation or approval issued by the competent authorities of the State in which th…
Biological samples transmitted by the medical biology laboratory established in France requesting the performance of the analytical phase are subject to a monitoring procedure making it possible to es…
Withdrawal of authorisation may be ordered by the Director General of the Regional Health Agency where it has been established, through an inspection carried out pursuant to Article L. 6231-1, that th…
At any time, the Minister for Health may request a copy of the laboratory's valid accreditation, authorisation or approval.
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