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Showing 7111–7120 of 13025 articles for “Art. Euronext Harmonised Market Rules — derivatives”
Persons manufacturing or marketing the substances, plants, medicinal products and other products mentioned in article R. 5132-98 shall, at their request, provide the Director General of the Agence nat…
…on procedure before a decision is taken on the granting, variation, suspension or withdrawal of the marketing authorisation, in particular on the basis of pharmacovigilance data.
…authorisation provided for in article R. 5141-86. This exemption does not apply to publications by marketing authorisation holders and companies exploiting veterinary medicinal products.
…ive to provide a report on the experience acquired with this device after it has been placed on the market.
…R. 5221-14 without displaying a sign clearly indicating that these devices may not be placed on the market or put into service until they have been brought into compliance is punishable by the fine la…
…out on all the health products mentioned in the first paragraph after they have been placed on the market.
The clerk of the court shall notify the president of the court of the filing of such application. The judgment shall not be enforceable and the court may not rule on the merits until a decision has be…
…ng the conditions laid down in article R. 214-32-25 ; b) They are entered into on regulated futures markets, the list of which is set by order of the Minister for the Economy, or meet the following cr…
…named patient of a medicinal product which does not have, whatever the therapeutic indication, of a marketing authorisation issued by the Agence nationale de sécurité du médicament et des produits de…
The rules of good practice that apply to the removal, preparation, preservation, transport and use of human body organs are drawn up by the Agence de la biomédecine after consultation with the Agence…
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