Article R6422-1
Leave to validate experience may be requested with a view to: 1° Taking part in the assessment session organised by the ministry or certifying body; 2° Preparing for the validation.
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Showing 5991–6000 of 52948 articles for “Art. CE 27-1-2017 n° 391817”
Leave to validate experience may be requested with a view to: 1° Taking part in the assessment session organised by the ministry or certifying body; 2° Preparing for the validation.
…aragraph:3° Each year, the activities of the Overseas Agency for Mobility and Adapted Military Service in the local authority ;4° Each year, a report on the activities of the Departmental Council, the…
In addition to the powers vested in the regional committee by articles R. 6123-3 to R. 6123-3-2, the committee in each of the local authorities mentioned in article R. 6523-15 is responsible for :a) I…
…ecutive Council in Martinique, the Regional Committee for Employment, Training and Vocational Guidance is made up of members appointed by order of the Prefect: 1° Eight representatives of the State: a…
Section 2 of Chapter III of Title II of Book I of this Part applies in Guadeloupe, French Guiana, Martinique and La Réunion subject to the provisions of this sub-section.
I. -Articles R. 6123-3-3, R. 6123-3-4 and R. 6123-3-10 do not apply. II.-For the application of article R. 6123-3-9, the words "national and" are deleted.
The declaration provided for in article L. 5131-2 shall be sent to the Agence nationale de sécurité du médicament et des produits de santé by a person authorised to bind the company to which the estab…
…nts may be reported: 1° A noxious and unintended reaction occurring during the use of a medical device in accordance with its intended purpose; 2° A noxious and unintended reaction resulting from the…
Reports are made :1° To the local materiovigilance correspondent when these reports are made by users or third parties who carry out their duties in one of the establishments or associations mentioned…
…r third parties who observe or are aware of incidents or risks of incidents involving a medical device. Third parties are considered to be persons who are neither manufacturers or their agents or user…
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