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Showing 891–900 of 69745 articles for “Art. s. R 743-140 and A 743-10”
A company operating a veterinary medicinal product must: 1° Keep detailed records of all suspected adverse reactions which have occurred inside or outside the European Union; 2° To record any suspecte…
The declaration and reporting obligations laid down in this section apply without prejudice to those laid down for veterinary medicinal products authorised by the European Medicines Agency in Regulati…
The procedures and standard form for the declarations and the periodic pharmacovigilance update report mentioned in articles R. 5141-103 to R. 5141-105-1 are laid down by decision of the Director Gene…
Without prejudice to the conditions laid down when the marketing authorisation is granted pursuant to the provisions of the fourth paragraph of Article L. 5141-5, the company operating the veterinary…
Notice for victims of road traffic accidents involving a land-based motor vehicle The following information is intended to explain what you need to do and how you will be compensated. It has been deli…
The sheet referred to in article L. 313-10 is provided to each borrower or co-borrower.
The provisions of this section apply to the establishments, services or organisations defined in Article L. 5126-10.
In addition to the treatments prescribed for a specific person, the establishments, services or organisations mentioned in I of article L. 5126-10 may hold certain medicines, products or objects menti…
The solvency calculation at the level of the group of insurance and reinsurance undertakings is carried out in accordance with the first method referred to in Article R. 356-19, based on consolidated…
Notwithstanding Article R. 8115-2, when the Regional Director for Business, Competition, Consumer Affairs, Labour and Employment decides to impose an administrative fine on the basis of Articles L. 47…
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