Article L5124-20
Any drug brokering activity carried out by a person located in France must be declared to the Agence nationale de sécurité du médicament et des produits de santé. Persons involved in the brokering of…
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Showing 4521–4530 of 6073 articles for “Art. 28 March 2012”
Any drug brokering activity carried out by a person located in France must be declared to the Agence nationale de sécurité du médicament et des produits de santé. Persons involved in the brokering of…
Failure by the person responsible for placing the tattooing product on the market, within the meaning of article L. 513-10-2, to report serious adverse reactions to the Agence nationale de sécurité du…
Persons legally established in another Member State of the European Union or party to the Agreement on the European Economic Area who wish to carry out on national territory on a temporary or occasion…
Copies or extracts of the minutes of the deliberations are certified by the Chairman of the Board of Directors, the Chief Executive Officer, the Deputy Chief Executive Officers, the Managing Director…
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…
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