Article D6221-34
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…
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Showing 4171–4180 of 46432 articles for “Art. D 223-2”
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.
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.
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.
I.-The full representatives mentioned in article D. 4422-30-2, in the event of their seat falling vacant due to death, resignation or loss of the capacity in respect of which they were elected, by the…
In the cases provided for in Article L. 2373-2, the following must be attached to the application for registration of the company resulting from the cross-border operation: 1° The agreement relating t…
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