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Showing 2431–2440 of 5619 articles for “Art. 13 nov. 2013”
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.
…exes; 2° The provisions of Articles 1 to 7 of Commission Implementing Regulation (EU) No 29/2012 of 13 January 2012, as amended, on marketing standards for olive oil ; 3° The provisions of Article 78…
…d down in Articles 28 to 30 of Commission Regulation (EU) 2018/273 of 11 December 2017 and Articles 13 to 20 of Commission Implementing Regulation (EU) 2018/274 of 11 December 2017 supplementing Regul…
…2014-158 of 20 February 2014 L. 511-12-1 Order no. 2015-1024 of 20 August 2015 L. 511-12-2 Law no. 2013-672 of 26 July 2013 L. 511-13 Order no. 2015-558 of 21 May 2015 L. 511-14 Order no. 2014-158 of…
…me table:Applicable articlesIn the wording resulting from the decreeR. 512-47 and R. 512-48no. 2014-1315 of 3 November 2014R. 512-49 and R. 512-50No. 2008-1262 of 4 December 2008R. 512-51n° 2013-938 o…
…same table:Applicable articlesIn the wording resulting from the decreeR. 512-47, R. 512-48no. 2014-1315 of 3 November 2014R. 512-49 and R. 512-50No. 2008-1262 of 4 December 2008R. 512-51n° 2013-938 o…
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