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Showing 5531–5540 of 9446 articles for “Art. D. n° 2004-1331”
…f administrative acts of the department and region in which each of the laboratory's sites is located.
…ation or approval issued by the competent authorities of the State in which the laboratory is located. If the declaration and attachments are not in French, they must be accompanied by a certified tra…
…n or approval issued by the competent authorities of the State in which the laboratory is established. If the declaration and attachments are not in French, they must be accompanied by a certified tra…
When a medical biology laboratory established in another Member State of the European Union or party to the Agreement on the European Economic Area and appearing on a list established by order of the…
The biological samples sent by the medical biology laboratory established in France requesting the analytical phase must be subject to a monitoring procedure to establish the conformity of the biologi…
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…
…shortcomings observed and has given him formal notice to put an end to them within a specified period. A copy of the formal notice is sent to the competent authorities of the State in which the labora…
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…
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