Effekten af GCP-direktivet på forskerinitierede kliniske laegemiddelforsøg--sekundaerpublikation

Research output: Contribution to journalJournal articleResearchpeer-review

  • Louise Berendt
  • Cecilia Håkansson
  • Karin Friis Bach
  • Kim Dalhoff
  • Per Buch Andreasen
  • Lene Birgitte Grejs Petersen
  • Elin Andersen
  • Poulsen, Henrik Enghusen
Since 2004, adherence to Good Clinical Practice has been mandatory for all clinical drug trials. This was new to the investigator-initiated trials. Our study showed no association between the implementation of the Directive and investigator or industry-initiated trials. However, a steady decline was observed over the entire period. Presumably, the introduction of GCP did not entail a decline because of the presence of GCP units at university hospitals. Thus, researchers can conduct clinical drug trials under the same regulations as drug companies.
Translated title of the contribution[Effect of the GCP Directive on academic drug trials]
Original languageDanish
JournalUgeskrift for Laeger
Volume170
Issue number33
Pages (from-to)2437-9
Number of pages3
ISSN0041-5782
Publication statusPublished - 11 Aug 2008

ID: 34090805