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Showing 1271–1280 of 9933 articles for “Art. EU Mutual Assistance Directive 2010/24/EU”
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. - Where an authority of another Member State of the European Union or party to the Agreement on the European Economic Area responsible for the supervision of a group on a consolidated basis consult…
Where an institution carrying on business in another Member State of the European Union or in another State party to the Agreement on the European Economic Area, in accordance with Articles L. 511-27…
…mined by a delegated act of the Commission adopted pursuant to paragraphs 3 and 5 of Article 260 of Directive 2009/138/EC of the European Parliament and of the Council of 25 November 2009 (Solvency II…
…mined by a delegated act of the Commission adopted pursuant to paragraphs 4 and 5 of Article 227 of Directive 2009/138/EC of the European Parliament and of the Council of 25 November 2009 (Solvency II…
…Article D. 533-4, the words: "referred to in the first paragraph of paragraph 1 of II of Annex 2 of Directive 2014/65/EU of 15 May 2014," and the words: "in accordance with Article 71(4) of Commission…
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