Article L4433-20
The regions of Guadeloupe, Mayotte and Réunion are consulted on the operating programmes and fare changes submitted by French companies for State approval for air and sea routes serving these regions.…
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Showing 6651–6660 of 17465 articles for “Art. Form 2044 spéciale”
The regions of Guadeloupe, Mayotte and Réunion are consulted on the operating programmes and fare changes submitted by French companies for State approval for air and sea routes serving these regions.…
The regions of Guadeloupe, Mayotte and Reunion define the actions they intend to carry out in terms of housing, following the opinion or, where appropriate, the proposal of the local authorities, the…
In the overseas departments and regions, the representative of the State in the region organises a consultation with the department and the region with a view to determining the local authority benefi…
For requests for substantial changes to the list of investigation sites or principal investigators, the Chairman issues the opinion on behalf of the Committee on the proposal of a single rapporteur.
…onditions provided for in 1 of Article 98 of the above-mentioned Regulation of 16 April 2014, may inform the designated personal protection committee within twenty-four hours that this application has…
The sponsor of a clinical trial which consists of the extension of a previous trial may inform the designated personal data protection committee within twenty-four hours that this trial is linked to a…
When an application for a substantial amendment to an initial clinical trial is submitted, the competent Committee for the Protection of Individuals shall carry out the Part II assessment provided for…
…in Article 17(5) of this Regulation. If the competent authority has sent a request for additional information to the sponsor, the personal data protection committee may forward observations relating t…
Applications for substantial amendments are subject to a simplified assessment procedure. These applications are examined by a select committee made up of two representatives from each of the colleges…
After submission of the application for clinical trial assessment defined in Article 5(1) of Regulation (EU) No 536/2014 of the European Parliament and of the Council of 16 April 2004, a Data Protecti…
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