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Showing 3021–3030 of 69703 articles for “Art. I and II”
The obligations of notification to the National Agency for the Safety of Medicines and Health Products or of information incumbent, under the vigilance exercised over the devices mentioned in Article…
For the devices mentioned in Article 1 of Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017, the list of which is set by decision of the Director General of the Ag…
Certain medical devices for individual use appearing on a list drawn up by order of the ministers responsible for health and social security may be returned to a state of good repair with a view to re…
Unless otherwise provided, the terms and conditions for the application of this chapter shall be laid down by decree in the Conseil d'Etat.
The victim informs the Office of any legal proceedings that may be in progress. If legal action is taken, the victim informs the judge that the matter has been referred to the Office. Victims only hav…
The Office is required to make an offer of compensation to any victim referred to in article L. 3122-1 within a period set by decree, which may not exceed six months from the date on which the Office…
Victims of losses resulting from contamination by the human immunodeficiency virus caused by a transfusion of blood products or an injection of blood-derived products carried out on the territory of t…
The Office is subrogated, up to the amount of the sums paid, to the rights that the victim has against the person responsible for the loss or damage as well as against the persons obliged in any way t…
In their claim for compensation, victims or their heirs must provide proof of having been infected by the human immunodeficiency virus and of having received transfusions of blood products or injectio…
It is forbidden to prescribe medicines classified as narcotics or subject to narcotics regulations for treatment lasting more than twenty-eight days.This period may be reduced for certain designated m…
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