Article R5121-148
The presence of an information leaflet for the user in the packaging of any medicinal product or product is compulsory, unless the information referred to in article R. 5121-149 appears directly on th…
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Showing 2351–2360 of 33248 articles for “Art. R 315-12”
The presence of an information leaflet for the user in the packaging of any medicinal product or product is compulsory, unless the information referred to in article R. 5121-149 appears directly on th…
The marketing authorisation holder must comply with the good package leaflet practices established by decision of the Director General of the Agence nationale de sécurité du médicament et des produits…
The package leaflet is drawn up in accordance with the summary of product characteristics. It includes a standard text, expressly inviting patients to report any suspected adverse reaction to their do…
In application of Article L. 641-15, the liquidator may, by order of the juge-commissaire, ask the legal representative of the legal entity or the debtor who is a natural person or any other employee…
In addition to the quarterly information mentioned in article L. 641-7, the liquidator shall submit at any time, at their request, and at least by 31 December each year, to the juge-commissaire and th…
Unless otherwise provided in this Title, the regulatory provisions relating to actions that fall within the jurisdiction of the mandataire judiciaire shall apply when they are pursued or brought by th…
Where the debtor practises a liberal profession subject to a legislative or regulatory status or whose title is protected, the court shall designate, when the proceedings are opened, the representativ…
The liquidator may operate the debtor's bank accounts under his signature for a period of six months from the judgment pronouncing the liquidation or, beyond that, for the duration of the continuation…
The list of claims mentioned in I of Article L. 641-13, brought to the attention of the administrator where one has been appointed or of the liquidator, pursuant to IV of the same article, shall be fi…
An order of the Minister for Health, issued on a proposal from the Director General of the Agence nationale de sécurité du médicament et des produits de santé, specifies the conditions for applying th…
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