Article L5431-8
The failure of the responsible person, as defined in Article 4 of Regulation (EC) No 1223/2009 of the European Parliament and of the Council of 30 November 2009, and distributors, as defined in Articl…
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Showing 8231–8240 of 50078 articles for “Art. I-7°”
The failure of the responsible person, as defined in Article 4 of Regulation (EC) No 1223/2009 of the European Parliament and of the Council of 30 November 2009, and distributors, as defined in Articl…
Any person involved in the manufacture, use, import, export or wholesale distribution of blood-derived medicinal products who fails to record the data required to monitor them pursuant to 14° of artic…
Attempted offences under articles L. 5421-2 and L. 5421-3 are punishable by the same penalties.
The following are empowered to investigate and record infringements and breaches of the provisions of Title I of Book II of this Part, as set out in Articles L. 5461-2 to L. 5461-9, as well as the reg…
Legal entities declared criminally liable, under the conditions set out inarticle 121-2 of the French Criminal Code, for the offences set out in this Title shall incur, in addition to the fine set out…
I. - It is an offence to market, broker or distribute, whether free of charge or against payment, wholesale or retail, homeopathic medicinal products mentioned in 11° of article L. 5121-1 or tradition…
Legal entities declared criminally liable, under the conditions set out in Article 121-2 of the French Penal Code, for the offences defined in Article L. 5431-2 shall be liable, in addition to a fine…
As part of this mission, the inspectors referred to in article L. 5411-1 may seize products on the basis of a judicial authorisation issued by an order of the liberty and custody judge. The request mu…
The following is punishable by two years' imprisonment and a fine of €30,000: 1° For any person who manufactures or packages cosmetic products, to open or operate an establishment for the manufacture…
Failure by any person exploiting a medicinal product or product to communicate any new information likely to influence the assessment of the benefits and risks of the medicinal product or product conc…
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