Article D6221-28
For the application of 4° and 5° of I ofArticle 7 of Order no. 2010-49 of 13 January 2010 as amended relating to medical biology, at least one examination per family of medical biology examinations sh…
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Showing 1081–1090 of 29092 articles for “Art. 20 mai 2010”
For the application of 4° and 5° of I ofArticle 7 of Order no. 2010-49 of 13 January 2010 as amended relating to medical biology, at least one examination per family of medical biology examinations sh…
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…
…that it has obtained accreditation for the various percentages set out in I ofArticle 7 of Order No 2010-49 of 13 January 2010 as amended relating to medical biology, enclosing a detailed list of the…
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…
The head of the medical biology laboratory established in another Member State of the European Union or party to the Agreement on the European Economic Area shall inform the Minister responsible for h…
The Minister for Health shall maintain and make available to the public a register of laboratories that have made the declaration provided for in the second paragraph of Article L. 6211-2-1 as it stoo…
…nd paragraph of Article L. 6211-2-1, as it stood prior to the entry into force of amended Order No. 2010-49 of 13 January 2010 relating to medical biology, shall be sent by the laboratory to the Minis…
The experts mentioned in articles D. 6221-30 and D. 6221-37 are appointed by order of the Minister for Health.
…atory are recognised as equivalent to those imposed by the first paragraph ofArticle 7 of Order no. 2010-49 of 13 January 2010 as amended relating to medical biology on laboratories established on Fre…
…cal samples accepted by the laboratory carrying out the analytical phase, their identification, the maintenance of their integrity and their traceability.
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