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Showing 5541–5550 of 9446 articles for “Art. D. n° 2004-1331”
The competent authorities of the State in which the laboratory has its registered office are informed of the decision of the Minister for Health.
…n or approval issued by the competent authorities of the State in which the laboratory is established. The application for authorisation and the attached documents must be accompanied by a certified t…
Biological samples transmitted by the medical biology laboratory established in France requesting the performance of the analytical phase are subject to a monitoring procedure making it possible to es…
Withdrawal of authorisation may be ordered by the Director General of the Regional Health Agency where it has been established, through an inspection carried out pursuant to Article L. 6231-1, that th…
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…
Renewal applications follow the same procedure as initial applications.
The list of Member States of the European Union or parties to the Agreement on the European Economic Area in which the accreditation conditions, the authorisation conditions or the approval conditions…
I.-The external quality assessment bodies referred to in article L. 6221-9 must meet the following criteria: 1° Competence, in terms of qualifications and experience, to organise quality control campa…
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