Avoiding rejections by European ethics committees
- PMID: 12852119
Avoiding rejections by European ethics committees
Abstract
The Competent Authority has been notified. The clinical investigator is anxious to begin. Just when the process of conducting a clinical investigation is proceeding as planned, the ethics committee issues an unfavourable opinion. This article discusses the actions that should be taken to avoid this occurrence and how to meet other requirements related to ethics committees.
Similar articles
-
Informed consent for a device investigation.IEEE Eng Med Biol Mag. 2004 May-Jun;23(3):97-8. doi: 10.1109/memb.2004.1317990. IEEE Eng Med Biol Mag. 2004. PMID: 15355002 No abstract available.
-
Clinical Trials Legislation - preparing for the revision of the European Directive Scheduled for 2011.Therapie. 2010 Jul-Aug;65(4):301-8, 291-9. doi: 10.2515/therapie/2010038. Epub 2010 Sep 21. Therapie. 2010. PMID: 20854751 Review. English, French.
-
Multicentre trials review process by research ethics committees in Spain: where do they stand before implementing the new European regulation?J Med Ethics. 2005 Jun;31(6):344-50. doi: 10.1136/jme.2003.007492. J Med Ethics. 2005. PMID: 15923484 Free PMC article.
-
Conducting clinical studies in Italy.Med Device Technol. 2005 Oct;16(8):21-4. Med Device Technol. 2005. PMID: 16355966
-
[Research ethics and revised law regarding the Danish Central Scientific Ethical Committee].Ugeskr Laeger. 2004 Jun 7;166(24):2337-40. Ugeskr Laeger. 2004. PMID: 15281571 Review. Danish. No abstract available.
MeSH terms
LinkOut - more resources
Medical