Article A385-2
The projection according to the scenario mentioned in a of I of article R. 385-4 is carried out over the ten financial years following the end of the previous financial year and according to the follo…
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Showing 3441–3450 of 13025 articles for “Art. Euronext Harmonised Market Rules — derivatives”
The projection according to the scenario mentioned in a of I of article R. 385-4 is carried out over the ten financial years following the end of the previous financial year and according to the follo…
I. - The preference shares included in the solvency margin referred to in 1° of I of article R. 385-1 must meet the following conditions:a) These securities carry financial rights defined by the artic…
A payment instrument is considered to be reserved for small-value payments when the deposit account agreement or the framework contract for payment services relating to that instrument specifies :- it…
For the purposes of Article L. 133-9, the payment service provider may set a cut-off time close to the end of a business day after which any payment order received is deemed to have been received on t…
…lated taking into account the current value of the underlying assets, the counterparty risk, future market trends and the time available to liquidate positions. For feeder UCITS, this calculation also…
…diate packaging and the outer packaging of a veterinary medicinal product which is the subject of a marketing authorisation must include the following information, in accordance with the marketing aut…
…e I of Part Two of the same Regulation. III.Liabilities arising from debt instruments with embedded derivatives such as structured notes that meet the conditions set out in I, with the exception of Ar…
…and establishments authorised under articles L. 4211-9-1 and L. 4211-9-2 may procure tissues, their derivatives and cells from the human body, whatever their level of processing, in a Member State of…
The correspondent mentioned in article R. 5121-181 who receives the report provided for in article R. 5121-196 immediately forwards it to the regional pharmacovigilance centre. If he is otherwise awar…
After the marketing authorisation has been granted, the marketing authorisation holder must immediately forward to the National Agency for the Safety of Medicines and Health Products, indicating the s…
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