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Showing 7751–7760 of 13025 articles for “Art. Euronext Harmonised Market Rules — derivatives”
…or direct application to humans or animals governed by EU Regulation 528/2012 on the placing on the market and use of biocidal products.
…and its components; 6° Substances and mixtures intended for research and development which are not marketed to the general public; 7° Waste governed by Title IV of Book V of the Environmental Code.
…et out in the aforementioned annexes, in particular with regard to the delimitation of the relevant markets, it requests that the file be completed or rectified.Acknowledgement of receipt of the compl…
…sional activity, whether or not it is intentionally produced and whether or not it is placed on the market.
…accuracy and truthfulness of the documents and data supplied to the Agency when the application for marketing authorisation is submitted and during its examination. The applicant must inform the Agenc…
…studies for a period of one year. In this case, the Director General of the Agency shall inform the marketing authorisation holder that the data from these studies are protected for a period of one ye…
…on (EC) No 1234/2008 of 28 November 2008 concerning the examination of variations to the terms of a marketing authorisation for medicinal products for human use and veterinary medicinal products, in a…
The marketing authorisation, the early access authorisation under 1° of II of article L. 5121-12 or the compassionate access authorisation under II of article L. 5121-12-1 or the compassionate prescri…
…e applicable, its colour. The manufacturer or the person responsible for placing the product on the market must respond to this request within three weeks of receipt. It keeps all requests and respons…
…nale de sécurité sanitaire de l'alimentation, de l'environnement et du travail or the applicant for marketing authorisation may refer the matter to the European Medicines Agency with a view to the app…
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