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Showing 7681–7690 of 14564 articles for “Art. 6 déc. 2004”
The manufacturer who intends to have clinical investigations carried out in France to verify the performance of a medical device or to detect any undesirable side effects, or his authorised representa…
As part of the procedure applicable to medical devices undergoing clinical investigations, the manufacturer shall draw up a declaration containing the information referred to in Articles R. 1123-37 to…
Implantable medical devices, active implantable medical devices and class III devices must be subject to clinical investigations, unless the use of existing clinical data can be duly justified.
As part of the procedure applicable to in vitro diagnostic medical devices undergoing an assessment of their performance, the manufacturer must draw up a declaration containing the data enabling the d…
…qualisation allocation made up of the urban equalisation allocation provided for in article L. 3334-6-1 and the minimum operating allocation provided for in article L. 3334-7.From 2005, the annual inc…
…andards of protection at least as stringent as the health safety rules mentioned in Article L. 1211-6. They also ensure that these elements or products are accompanied by the information mentioned in…
Without prejudice to the information obligations provided for in article 19 of law no. 2004-575 of 21 June 2004 for confidence in the digital economy and in articles L. 111-7 and L. 111-7-1 of this co…
…r residential purposes, built before 1 January 1949, within four years of the date on which Act no. 2004-806 of 9 August 2004 on public health policy comes into force.
I. - Pursuant to Article 7, 8° of Organic Law No. 2004-192 of 27 February 2004, subject to the provisions of II, Articles R. 151-1 to R. 151-17 are automatically applicable in French Polynesia.II. - F…
…contracting authorities or entities in the fields of defence and security, and amending Directives 2004/17/EC and 2004/18/EC," are deleted;4° In Article L. 2341-1, the references to articles 1741 to…
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