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Complying with the European Clinical Trials directive while surviving the administrative pressure - an alternative approach to toxicity registration in a cancer trial

Thomas Leth Frandsen, Mats Heyman, Jonas Abrahamsson, Kim Vettenranta, Ann Åsberg, Goda Vaitkeviciene, Kaie Pruunsild, Nina Toft, Henrik Birgens, Helena Hallböök, Petter Quist-Paulsen, Laimonas Griškevičius, Louise Helt, Birgitte Vilsbøll Hansen, Kjeld Schmiegelow

76 Citations (Scopus)

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