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Journal Abstract Search
259 related items for PubMed ID: 17138913
21. United States regulatory requirements for research involving human subjects. J Biolaw Bus; 1998; 1(2):39-53. PubMed ID: 12739542 [No Abstract] [Full Text] [Related]
25. Understanding informed consent for participation in international health research. Jegede AS. Dev World Bioeth; 2009 Aug; 9(2):81-7. PubMed ID: 18637943 [Abstract] [Full Text] [Related]
26. The International Xenotransplantation Association consensus statement on conditions for undertaking clinical trials of porcine islet products in type 1 diabetes--chapter 7: Informed consent and xenotransplantation clinical trials. Vanderpool HY. Xenotransplantation; 2009 Aug; 16(4):255-62. PubMed ID: 19799766 [Abstract] [Full Text] [Related]
31. Informed consent and collaborative research: perspectives from the developing world. Hyder AA, Wali SA. Dev World Bioeth; 2006 Mar; 6(1):33-40. PubMed ID: 16436172 [Abstract] [Full Text] [Related]
33. Proposal for a good clinical practice directive. European Commission. Bull Med Ethics; 1998 Feb; No. 135():6-11. PubMed ID: 11657249 [No Abstract] [Full Text] [Related]
35. [The newly revised Declaration of Helsinki: what do the changes mean from an ethical perspective?]. Rid A, Schmidt H. Dtsch Med Wochenschr; 2009 Dec; 134(49):2525-8. PubMed ID: 19941238 [Abstract] [Full Text] [Related]
36. Ethical and regulatory challenges associated with the exception from informed consent requirements for emergency research: from experimental design to institutional review board approval. Vaslef SN, Cairns CB, Falletta JM. Arch Surg; 2006 Oct; 141(10):1019-23; discussion 1024. PubMed ID: 17043281 [Abstract] [Full Text] [Related]