Article R5121-146
The labelling and, where applicable, the package leaflet of the medicinal products referred to in article L. 5121-13 must bear the following information only: 1° Homeopathic medicinal product in clear…
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Showing 9171–9180 of 10732 articles for “Art. BOI-ENR-DMTG-10-10-20-20 n° 380”
The labelling and, where applicable, the package leaflet of the medicinal products referred to in article L. 5121-13 must bear the following information only: 1° Homeopathic medicinal product in clear…
I.-Family information, consultation or counselling establishments carry out the following tasks:1° To provide information about rights relating to emotional, relational and sexual life and to educate…
I. - The General Regulation of the Autorité des marchés financiers sets the conditions under which any natural person or legal entity who is a shareholder of a company whose registered office is locat…
I - The value of the prudential technical provisions referred to in Article L. 351-2 is equal to the sum of the best estimate and the risk margin. II - The best estimate corresponds to the probability…
The basis of assessment for real estate wealth tax is the net value at 1 January of the year: 1° Of all the property and property rights belonging to the persons mentioned in article 964 as well as to…
The professional practice standard relating to audit planning, approved by the Minister of Justice, is shown below: . NEP-300. Audit planning Introduction 01. The audit of the accounts carried out by…
Pursuant to the third paragraph of Article L. 561-46, the persons with access to all information relating to beneficial owners are as follows: 1° Judicial officers, for the purposes of carrying out th…
PART I: Basic equation expressing the equivalence of loans, on the one hand, and repayments and charges, on the other. The basic equation, which defines the annual percentage rate of charge (APR), exp…
1. a. Taxpayers domiciled in France for tax purposes, within the meaning of the article 4 B, are entitled to an income tax reduction equal to 30% of payments made up to 31 December 2024 in respect of…
I.- Clinical trials of medicinal products are governed by the provisions of Regulation (EU) No 536/2014 of the European Parliament and of the Council of 16 April 2014. The competent authority for carr…
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