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Showing 4581–4590 of 62443 articles for “Art. comité juridique of 3 December 2008”
…levant information available, without prejudice to their respective responsibilities and regardless of whether or not they are established in the same Member State, the Autorité de contrôle prudentiel…
…y are accompanied by a complete file. The application is deemed to be complete if, within one month of receipt, the Minister for Health has not informed the applicant, by registered letter with acknow…
The head of the medical biology laboratory established in another Member State of the European Union or party to the Agreement on the European Economic Area shall inform the Minister responsible for h…
The declaration provided for in the second paragraph of Article L. 6211-2-1, as it stood prior to the entry into force of amended Order No. 2010-49 of 13 January 2010 relating to medical biology, shal…
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…
…he Minister for Health will decide on the application for authorisation after receiving the opinion of the committee referred to in article L. 6213-12. His decision is published in the Journal officie…
The competent authorities of the State in which the laboratory has its registered office are informed of the decision of the Minister for Health.
At any time, the Minister for Health may request a copy of the laboratory's valid accreditation, authorisation or approval.
The application for authorisation must be accompanied, where appropriate, by a copy of the documents representing accreditation, authorisation or approval issued by the competent authorities of the St…
The authorisation is issued for a period of five years. It specifies the medical biology tests that the laboratory is authorised to carry out for patients resident in France.
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