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2. FDA's new rule on treatment use and sale of investigational new drugs. Levine RJ. IRB; 1987; 9(4):1-4. PubMed ID: 11649946 [No Abstract] [Full Text] [Related]
3. IRB review of a Phase II randomized clinical trial involving incompetent patients suffering from severe closed head injury. Prentice ED, Antonson DL, Leibrock LG, Kelso TK, Sears TD. IRB; 1993; 15(5):1-7. PubMed ID: 11659703 [No Abstract] [Full Text] [Related]
5. An IRB member's perspective on access to innovative therapy. Moore DL. Albany Law Rev; 1994; 57(3):559-81. PubMed ID: 11652854 [No Abstract] [Full Text] [Related]
6. Institutional review boards in the university setting: review of pharmaceutical testing protocols, informed consent and ethical concerns. Kobasic DM. J Coll Univ Law; 1988; 15(2):185-216. PubMed ID: 11659168 [No Abstract] [Full Text] [Related]
10. Multicenter trials and subject eligibility: should local IRBs play a role? Freedman B. IRB; 1994; 16(1-2):1-6. PubMed ID: 11652320 [No Abstract] [Full Text] [Related]
11. Considering experimentation and elusive truth: informed consent made difficult. Brodeur D. Issues (St Louis Mo); 1992; 7(2):1-8. PubMed ID: 11659444 [No Abstract] [Full Text] [Related]
15. IRB review of adverse events in investigational drug studies. Prentice ED, Gordon B. IRB; 1997; 19(6):1-4. PubMed ID: 11656910 [No Abstract] [Full Text] [Related]