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Showing 5391–5400 of 54001 articles for “Art. I-4°”
As part of the EC declaration of conformity procedure, product quality assurance, the manufacturer shall submit to an authorised body for verification the quality system which he has set up for the fi…
As part of the procedure for the EC declaration of conformity, a full quality assurance system, the manufacturer must submit to an approved body for verification the quality system which he has set up…
As part of the procedure for the EC declaration of conformity, product quality assurance, for class II b medical devices, the manufacturer must submit an application to the authorized body for assessm…
The emergency medical aid services may participate in the medical coverage of large gatherings in accordance with the procedures laid down by the police authorities concerned after consulting the dire…
The protocol referred to in Article R. 6411-3 defines in particular, in compliance with the regulations to which the prison is subject: 1° The conditions under which the staff of the public health est…
Any joint stock company participating in a merger operation shall make the following documents available to its shareholders at its registered office at least thirty days before the date on which the…
In order to examine the project, the responsible minister(s) may call upon the services of another minister, a public interest grouping or a public establishment, in compliance with the legislative an…
For the purposes of this Book, the supervising minister is:1° The minister or ministers exercising supervision pursuant to the legislative or regulatory texts in force;2° For public interest groupings…
Draft partnership contracts concluded on behalf of unauthorised purchasers are examined by the responsible minister.
The brand name and trade name may be printed on cigarette paper in accordance with the procedures defined by order of the Minister for Health.
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