Typical investigational medicinal products follow relatively uniform regulations in 10 European Clinical Research Infrastructures Network (ECRIN) countries

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

  • Christian Gluud
  • Christine Kubiak
  • Kate Whitfield
  • Jane Byrne
  • Karl-Heinz Huemer
  • Christian Libersa
  • Béatrice Barraud
  • Xina Grählert
  • Gabriele Dreier
  • Sebastian Geismann
  • Wolfgang Kuchinke
  • Zsuza Temesvari
  • Gyorgy Blasko
  • Gabriella Kardos
  • Timothy O'Brien
  • Margaret Cooney
  • Siobhan Gaynor
  • Arrigo Schieppati
  • Fernando de Andres
  • Nuria Sanz
  • German Kreis
  • Charlotte Asker-Hagelberg
  • Hanna Johansson
  • Sue Bourne
  • Adeeba Asghar
  • Jean-Marc Husson
  • Jacques Demotes-Mainard
In order to facilitate multinational clinical research, regulatory requirements need to become international and harmonised. The EU introduced the Directive 2001/20/EC in 2004, regulating investigational medicinal products in Europe.
OriginalsprogEngelsk
TidsskriftTrials
Vol/bind13
Sider (fra-til)27
ISSN1745-6215
DOI
StatusUdgivet - 2012

ID: 48998962