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Journal Abstract Search
267 related items for PubMed ID: 6846357
21. Trials and errors: barriers to oversight of research conducted under the emergency research consent waiver. Kipnis K, King NM, Nelson RM. IRB; 2006; 28(2):16-9. PubMed ID: 16770884 [No Abstract] [Full Text] [Related]
22. ASHP professional policy recommendations--Invitation to comment. Am J Health Syst Pharm; 2010 Apr 15; 67(8):e5-10. PubMed ID: 20360574 [No Abstract] [Full Text] [Related]
23. The IRB's role in assessing the generalizability of non-NIH-funded clinical trials. Weijer C. IRB; 1998 Apr 15; 20(2-3):1-5. PubMed ID: 11656912 [No Abstract] [Full Text] [Related]
24. Biotech and pharma face more costly clinical trials. Brower V. Nat Biotechnol; 1998 Aug 15; 16(8):714. PubMed ID: 9702762 [No Abstract] [Full Text] [Related]
25. Mission, role, and functions of the P & T Committee. Bell JE, Evans PJ, Standish RC. Hosp Formul; 1983 Jun 15; 18(6):639-40, 643-6. PubMed ID: 10260202 [Abstract] [Full Text] [Related]
26. IRB review of adverse events in investigational drug studies. Prentice ED, Gordon B. IRB; 1997 Jun 15; 19(6):1-4. PubMed ID: 11656910 [No Abstract] [Full Text] [Related]
27. The changing clinical trials scene: the role of the IRB. Mitchell SC, Steingrub J. IRB; 1988 Jun 15; 10(4):1-5. PubMed ID: 11650078 [No Abstract] [Full Text] [Related]
28. Clinical trials face heightened scrutiny as science and commerce appear to merge. Lorman AJ. J Biolaw Bus; 2001 Jun 15; 4(4):23-32. PubMed ID: 12751494 [Abstract] [Full Text] [Related]
29. FDA seeks tighter controls over research with human subjects. Hershey N, Miller RD. Hosp Med Staff; 1978 Dec 15; 7(12):1-7. PubMed ID: 10239337 [Abstract] [Full Text] [Related]
30. Procedures for emergency or treatment use of investigational drugs. Klecker RJ, Cipolle RJ. Am J Hosp Pharm; 1987 May 15; 44(5):1086-9. PubMed ID: 3605118 [Abstract] [Full Text] [Related]
31. JCAHO--clinical indicators--a glimpse into the future. Hoffmann RP. Hosp Pharm; 1989 Jan 15; 24(1):63-4. PubMed ID: 10291603 [No Abstract] [Full Text] [Related]
32. Individual researcher liability for clinical research on humans. Miller RK. J Biolaw Bus; 2003 Jan 15; 6(2):8-16. PubMed ID: 14682365 [Abstract] [Full Text] [Related]
33. ASHP guidelines on preventing medication errors with chemotherapy and biotherapy. Goldspiel B, Hoffman JM, Griffith NL, Goodin S, DeChristoforo R, Montello CM, Chase JL, Bartel S, Patel JT. Am J Health Syst Pharm; 2015 Apr 15; 72(8):e6-e35. PubMed ID: 25825193 [No Abstract] [Full Text] [Related]
34. Clinical trials. Agency wants to stop shopping for best deal. Malakoff D. Science; 2002 Jun 14; 296(5575):1953. PubMed ID: 12065814 [No Abstract] [Full Text] [Related]
35. Paediatric clinical trials: redressing the imbalance. Schreiner MS. Nat Rev Drug Discov; 2003 Dec 14; 2(12):949-61. PubMed ID: 14654794 [No Abstract] [Full Text] [Related]
36. The FDA's enforcement of IRBs and patient informed consent. Kelsey FO. Food Drug Cosmet Law J; 1989 Jan 14; 44(1):13-20. PubMed ID: 11651627 [No Abstract] [Full Text] [Related]
37. Informed consent: the FDA's perspective. Bagley G. Food Drug Law J; 1993 Jan 14; 48(2):181-6. PubMed ID: 11653141 [No Abstract] [Full Text] [Related]
38. International research agreement leads to new U.S. guidelines. Maloney DM. Hum Res Rep; 1995 Apr 14; 10(4):1-2. PubMed ID: 11654182 [No Abstract] [Full Text] [Related]
39. Controlling investigational drug use in community hospitals. Chase PA. Am J Hosp Pharm; 1991 Jan 14; 48(1):61-2. PubMed ID: 2000874 [No Abstract] [Full Text] [Related]
40. The Food and Drug Administration perspective: use of an investigational drug in a medical emergency. Schultheis LW, Rappaport BA. Anesth Analg; 2007 Mar 14; 104(3):479-80. PubMed ID: 17312189 [No Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]