216 related articles for article (PubMed ID: 17914035)
1. Open clinical trials.
Drazen JM; Morrissey S; Curfman GD
N Engl J Med; 2007 Oct; 357(17):1756-7. PubMed ID: 17914035
[No Abstract] [Full Text] [Related]
2. Progress and deficiencies in the registration of clinical trials.
Wood AJ
N Engl J Med; 2009 Feb; 360(8):824-30. PubMed ID: 19228628
[No Abstract] [Full Text] [Related]
3. Data from human research projects will now be available to public.
Maloney DM
Hum Res Rep; 2001 Apr; 16(4):1-2. PubMed ID: 11883453
[No Abstract] [Full Text] [Related]
4. Making clinical data widely available.
Kaiser J
Science; 2008 Oct; 322(5899):217-8. PubMed ID: 18845745
[No Abstract] [Full Text] [Related]
5. Safeguarding clinical trials.
Nat Med; 2007 Feb; 13(2):107. PubMed ID: 17290249
[No Abstract] [Full Text] [Related]
6. The web of clinical trial registration obligations: have foreign clinical trials been caught?
Hathaway CR; Manthei JR; Haas JB; Meltzer ED
Food Drug Law J; 2009; 64(2):261-75. PubMed ID: 19999283
[TBL] [Abstract][Full Text] [Related]
7. Clinical trials registries: towards improved access to therapeutic data.
Prescrire Int; 2008 Dec; 17(98):256-9. PubMed ID: 19425275
[TBL] [Abstract][Full Text] [Related]
8. Public registration of clinical trials.
Steinbrook R
N Engl J Med; 2004 Jul; 351(4):315-7. PubMed ID: 15269307
[No Abstract] [Full Text] [Related]
9. Ethical and scientific implications of the globalization of clinical research.
Andrews CA
N Engl J Med; 2009 Jun; 360(26):2793; author reply 2793. PubMed ID: 19557890
[No Abstract] [Full Text] [Related]
10. Looking abroad: clinical drug trials.
Hathaway CR; Manthei JR; Haas JB; Scherer CA
Food Drug Law J; 2008; 63(3):673-81. PubMed ID: 19031667
[No Abstract] [Full Text] [Related]
11. [Regulations concerning data transparency- a comparison between the USA and Europe].
Quack C
Z Evid Fortbild Qual Gesundhwes; 2011; 105(3):183-8. PubMed ID: 21530907
[TBL] [Abstract][Full Text] [Related]
12. Recruiting human subjects without IRB review/approval.
Maloney DM
Hum Res Rep; 2002 Aug; 17(8):3. PubMed ID: 12731493
[No Abstract] [Full Text] [Related]
13. Gene therapy for rare diseases.
Nat Genet; 1999 Aug; 22(4):313-4. PubMed ID: 10431225
[No Abstract] [Full Text] [Related]
14. Protecting research subjects--what must be done.
Shalala D
N Engl J Med; 2000 Sep; 343(11):808-10. PubMed ID: 10984573
[No Abstract] [Full Text] [Related]
15. Improving protection for research subjects.
Steinbrook R
N Engl J Med; 2002 May; 346(18):1425-30. PubMed ID: 11986426
[No Abstract] [Full Text] [Related]
16. New FDA regulation to improve safety reporting in clinical trials.
Sherman RB; Woodcock J; Norden J; Grandinetti C; Temple RJ
N Engl J Med; 2011 Jul; 365(1):3-5. PubMed ID: 21651388
[No Abstract] [Full Text] [Related]
17. The globalization of clinical trials: a growing challenge in protecting human subjects: executive summary (2001).
Department of Health and Human Services, Office of the Inspector General, USA
J Int Bioethique; 2003; 14(1-2):165-9. PubMed ID: 15035253
[No Abstract] [Full Text] [Related]
18. No-consent trials raise concern.
Dove A
Nat Med; 1999 Mar; 5(3):250-1. PubMed ID: 10086366
[No Abstract] [Full Text] [Related]
19. Predictable materiality: a need for common criteria governing the disclosure of clinical trial results by publicly-traded pharmaceutical companies.
Cohen K; Cormier JW; Davar MV
J Contemp Health Law Policy; 2013; 29(2):201-32. PubMed ID: 23837261
[No Abstract] [Full Text] [Related]
20. US plans to protect clinical research participants.
Fox JL
Nat Biotechnol; 2000 Jul; 18(7):709. PubMed ID: 10888829
[No Abstract] [Full Text] [Related]
[Next] [New Search]
