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Showing 7581–7590 of 28915 articles for “Art. Cons. conc. n° 91-D-42 du 22 Oct 1991”
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…
…m there and for which it is seeking authorisation; 2° The number of medical biology tests performed during the calendar year preceding the application; 3° The number of people working in the laborator…
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…
…ished in France requesting the performance of the analytical phase are subject to a monitoring procedure making it possible to establish the conformity of the biological samples accepted by the labora…
…danger to the safety of patients or persons working in the laboratory, he shall implement the procedure provided for in Article R. 6231-1.
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…
When it is established that the operating conditions of the laboratory established in another Member State of the European Union or party to the Agreement on the European Economic Area holding the aut…
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