Informed consent for a device investigation
- PMID: 15355002
- DOI: 10.1109/memb.2004.1317990
Informed consent for a device investigation
Similar articles
-
U.S. FDA rules for device investigations.IEEE Eng Med Biol Mag. 2003 Jan-Feb;22(1):95-6. doi: 10.1109/memb.2003.1191461. IEEE Eng Med Biol Mag. 2003. PMID: 12683070 No abstract available.
-
Avoiding rejections by European ethics committees.Med Device Technol. 2003 Jun;14(5):26-8. Med Device Technol. 2003. PMID: 12852119
-
Regulating clinical research: informed consent, privacy, and IRBs.Cap Univ Law Rev. 2003;31(1):71-91. Cap Univ Law Rev. 2003. PMID: 15295833 No abstract available.
-
Risk management of European device clinical studies.Med Device Technol. 2007 Mar-Apr;18(2):39-42. Med Device Technol. 2007. PMID: 17494500 Review.
-
Proxy and surrogate consent in geriatric neuropsychiatric research: update and recommendations.Am J Psychiatry. 2004 May;161(5):797-806. doi: 10.1176/appi.ajp.161.5.797. Am J Psychiatry. 2004. PMID: 15121642 Review.
MeSH terms
LinkOut - more resources
Full Text Sources
Medical