Genmab — April 2017
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er det ikke agenda for chmp kommitteen? det er kommissionen, der skal give godkendelsen. chmp har allerede gjort deres
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http://www.ema.europa.eu/ema/index.jsp?curl=pages/regulation/general/general_content_001595.jsp&mid=WC0b01ac0580b18a3d#Steps involved in obtaining an EU marketing authorisation
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det øverste link fungerede ikke - check i bunden af siden
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mandag 1. maj bør være den absolutte bagkant for approval beslutningen
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mon ikke de får lidt kolde fødder ved tanken om den acceleration dara viser i markedet - og det relativt tynde ansøgningsmateriale, der bliver sendt frem til dem?
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så kommer kl 1400 hugget igen på klokkeslet
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