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Showing 5011–5020 of 65336 articles for “Art. L 143-12 à L 143-15”
The relay doctor informs the doctor chosen by the person subject to the therapeutic injunction of the legal framework in which the injunction operates. This doctor confirms to the relay doctor, in wri…
After it has been issued, the parallel import authorisation may be suspended or withdrawn by the Director General of the Agence nationale de sécurité du médicament et des produits de santé if the medi…
1. When an individual domiciled in France holds directly or indirectly at least 10% of the shares, units, financial rights or voting rights in a legal entity-a legal person, body, trust or comparable…
The court judgment replaces the European order for payment.
Waste is transported and disposed of in accordance with current regulations.
Any health establishment or health cooperation group which uses or supplies medical devices or makes such devices available to its members, as well as any association distributing medical devices at h…
During the design, study and development of the project, the coordinator : 1° Draw up the general co-ordination plan when required; 2° Compile the file on subsequent work on the project; 3° Open a co-…
The procedure provided for in Article R. 4623-5 also applies: 1° In autonomous occupational health and prevention services, in the event of a change of sector or company in the group monitored by an o…
The application for renewal of the parallel import authorisation must be submitted no later than three months before the expiry date of the parallel import authorisation. It must be accompanied by a d…
The CE marking is affixed under the responsibility of the manufacturer or his authorised representative, in a visible, legible and indelible manner on the in vitro diagnostic medical device where this…
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