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Showing 2521–2530 of 5385 articles for “Art. 13 Nov 2008”
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.
…Code is replaced by the reference to the registration fees provided for inarticle 89 of decree no. 2008-1086 of 23 October 2008 relating to the registration of property rights in Mayotte.
…Directive 87/250/EEC, Council Directive 90/496/EEC, Commission Directive 1999/10/EC, Directive 2000/13/EC of the European Parliament and of the Council, Commission Directives 2002/67/EC and 2008/5/EC…
…f Article 11, paragraph 6 of Article 16 and Article 20 of amended Commission Regulation (EC) No 543/2008 of 16 June 2008 laying down detailed rules for implementing Council Regulation (EC) No 1234/200…
…monised standards in force applicable to medical biology laboratories, within the meaning ofarticle 137 of law no. 2008-776 of 4 August 2008 on the modernisation of the economy.
…set by collective agreements concluded after the date of publication of the aforementioned Act no. 2008-596 of 25 June 2008;-shorter periods fixed in the letter of engagement or the employment contra…
…ariations and extensions as defined in 3° and 4° of Article 2 of Commission Regulation (EC) No 1234/2008 of 28 November 2008 concerning the examination of variations to the terms of a marketing author…
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