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Showing 5591–5600 of 7327 articles for “Art. 18 March 2020”
I.-The treatment products and processes used to comply with the rules laid down in Article D. 1332-2 are authorised by the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement…
In the case of the creation of a new cinematographic entertainment establishment, the future operator of the establishment produces a file in support of its application comprising:
An electronic signature shall be validly affixed only by the use of a process that enables the signatory to be identified, guarantees the link between the signature and the document to which it relate…
Accreditations are issued by the French Accreditation Committee or by any other accreditation body designated pursuant to Regulation (EC) No 765/2008 of the European Parliament and of the Council of 9…
The marketing authorisation, the early access authorisation under 1° of II of article L. 5121-12 or the compassionate access authorisation under II of article L. 5121-12-1 or the compassionate prescri…
This sub-section applies to post-authorisation safety studies of a non-interventional nature within the meaning of Article R. 1121-2, which give rise to the collection of safety information from patie…
The holder of the parallel import authorisation is responsible for placing the product on the market and, in this capacity, ensures that the provisions of this Title are complied with, in particular t…
As part of the EC verification procedure, the manufacturer submits the devices manufactured for inspection by an authorised body. The authorised body checks the conformity of the medical devices with…
Poison control centres are responsible for responding, particularly in emergencies, to any request for risk assessment and any request for an opinion or advice concerning the diagnosis, prognosis and…
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