These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
6. New public health service regulations on human experimentation. Curran WJ N Engl J Med; 1969 Oct; 281(14):781-2. PubMed ID: 5807926 [No Abstract] [Full Text] [Related]
7. Bioethical malpractice: risk and responsibilities in human research. Noah BA J Health Care Law Policy; 2004; 7(2):175-241. PubMed ID: 15573441 [No Abstract] [Full Text] [Related]
8. Research involving children: regulations, review boards and reform. Gandhi R J Health Care Law Policy; 2005; 8(2):264-330. PubMed ID: 16471026 [No Abstract] [Full Text] [Related]
9. The regulation of clinical investigators. Endries RN Food Drug Cosmet Law J; 1980 Jul; 35(7):415-23. PubMed ID: 11661860 [No Abstract] [Full Text] [Related]
10. Conflicts of interest in medical research: how much conflict should exceed legal boundaries? Klanica K J Biolaw Bus; 2005; 8(3):37-45. PubMed ID: 16459426 [TBL] [Abstract][Full Text] [Related]
11. Protection of human subjects; proposed establishment of regulations. Fed Regist; 1979 Apr; 44(80):24106-11. PubMed ID: 10241036 [No Abstract] [Full Text] [Related]
12. Kelsey's Commandos: FDA investigates the investigators. Small WE Am Pharm; 1979 Jun; 19(6):30-3. PubMed ID: 463736 [No Abstract] [Full Text] [Related]
13. When do the federal regulations allow placebo-controlled trials in children? Miller FG; Wendler D; Wilfond B J Pediatr; 2003 Feb; 142(2):102-7. PubMed ID: 12584527 [No Abstract] [Full Text] [Related]
14. Protecting human research subjects and the public: the role of FDA disqualification of clinical investigators. Nightingale SL Food Drug Cosmet Law J; 1980 Sep; 35(9):484-92. PubMed ID: 11661914 [No Abstract] [Full Text] [Related]
15. Protection of human subjects: proposed regulations on research involving prisoners. Fed Regist; 1978 Jan; 43(3):1049-53. PubMed ID: 10306149 [No Abstract] [Full Text] [Related]
16. Researcher liability for negligence in human subject research: informed consent and researcher malpractice actions. Jansson RL Wash Law Rev; 2003 Feb; 78(1):229-63. PubMed ID: 15732212 [TBL] [Abstract][Full Text] [Related]
17. Protection of human subjects; informed consent; standards for institutional review boards for clinical investigations--FDA. Proposed rule. Fed Regist; 1988 Nov; 53(218):45678-82. PubMed ID: 10290533 [TBL] [Abstract][Full Text] [Related]
19. If a subject incurs obligations and carries them out, then consent is a contract: Dahl v. HEM Pharmaceuticals (Part II). Maloney DM Hum Res Rep; 1996 Jan; 11(1):4-5. PubMed ID: 11653221 [No Abstract] [Full Text] [Related]
20. FDA seeks tighter controls over research with human subjects. Hershey N; Miller RD Hosp Med Staff; 1978 Dec; 7(12):1-7. PubMed ID: 10239337 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]