Article R2131-2-B
…31-2-A defines the overall architecture of the chain for the remote transmission of acts subject to legality control as well as the characteristics required for the approval of a remote transmission s…
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Showing 3461–3470 of 12461 articles for “Art. legal committee”
…31-2-A defines the overall architecture of the chain for the remote transmission of acts subject to legality control as well as the characteristics required for the approval of a remote transmission s…
In the cases provided for in l'article L. 2221-7, the director of a public service company responsible for the operation of an industrial and commercial public service or the chairman of the board of…
…ative or judicial court. In this case, the Office will act as principal and may avail itself of all legal remedies.
Within one month of receipt of the letter referred to in Article R. 3122-21, the Office shall inform the president of the court concerned whether or not a claim for compensation with the same purpose…
Copies of decisions given at first instance and, where applicable, on appeal, in proceedings in which the Office is not involved are sent to the Office by the Registry or the Secretariat of the Regist…
…ent of receipt, a copy of the pleadings in which they are seised, initially or additionally, of any legal claim relating to compensation for the losses defined in the first paragraph of article L. 312…
The Director General of the Agence nationale de sécurité du médicament et des produits de santé may grant, under the conditions laid down in Article R. 5211-55 and Article 4 of Implementing Regulation…
The General Director of the Agence nationale de sécurité du médicament et des produits de santé regularly checks that the authorised body has the required skills and up-to-date knowledge of the medica…
Authorised bodies shall inform the Director General of the Agence nationale de sécurité du médicament et des produits de santé of all certificates issued, modified, supplemented, suspended, withdrawn…
The approved body may require the manufacturer to provide any information and to carry out any test or assessment necessary for it to carry out the verifications for which it is responsible.
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