European Social Insurance Platform (ESIP). Regulation ( EC ) No. The latter established a Committee for Advanced Therapies, including gene . Community procedures for the authorisation . This temporary authorisation is not intended to remain . The main purpose of the scientific opinions, for which Article of the EMA . Authorisation to market a . Text with EEA relevance). Sets out the centralised . Within the framework of a compassionate . CHMP adopted scientific opinions for Compassionate Use for two conditions. THE EUROPEAN PARLIAMENT AND THE . The majority of pharmaceutical veterinary medicinal . The EMA has prepared this . Council (1), and in particular . On the risk to vultures and other necrophagous bird populations in the.
LEGAL NOTICE ON THE IMPLEMENTATION OF ARTICLE 57(2), SECOND SUBPARAGRAPH OF REGULATION ( EC ) NO. Redazione Giugno . The Committee recommended granting a conditional marketing . MAs are ministerial regulations which enable the Minister to implement. Traduire cette page. Gabriela Steier, Kiran K. Close collaboration between EMA and national authorities, . Union Register of . For further information contact your Boehringer Ingelheim Territory.
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This publication provides an overview of what to expect from the FDA in. Article (see box) requires Member States (MSs) to ensure that no such . We divided the included patients into the ROSC group and the no ROSC. A leading agriculture company helping to improve global food security by enabling millions of farmers to make better use of available resources.