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Showing 6171–6180 of 9726 articles for “Art. D. 145-34”
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…
The medical biology laboratory shall inform the regional health agency within whose jurisdiction it is located electronically that it has obtained accreditation for the various percentages set out in…
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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