Article D6221-30
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…
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Showing 2541–2550 of 5457 articles for “Art. Dir. 93/13/EEC”
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…
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…
The 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 offici…
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.
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…
Renewal applications follow the same procedure as initial applications.
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