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2. 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]
3. International research agreement leads to new U.S. guidelines. Maloney DM Hum Res Rep; 1995 Apr; 10(4):1-2. PubMed ID: 11654182 [No Abstract] [Full Text] [Related]
4. The law relating to confidentiality of data acquired by researchers in the biomedical and social sciences. Bravender-Coyle P Univ Tasman Law Rev; 1986; 8(3):333-60. PubMed ID: 11650864 [No Abstract] [Full Text] [Related]
5. Guidelines for confidentiality in research on AIDS. Bayer R; Levine C; Murray TH IRB; 1984; 6(6):1-7. PubMed ID: 11649192 [No Abstract] [Full Text] [Related]
6. European directive on clinical trials. Bull Med Ethics; 1999 May; No. 148():3-4. PubMed ID: 11657983 [No Abstract] [Full Text] [Related]
7. Drug industry lobbies against European research-data directive. Mitchell P Lancet; 1997 May; 349(9062):1378. PubMed ID: 11655134 [No Abstract] [Full Text] [Related]
8. A regulatory overview of alternatives to animal testing: United States, Europe, and Japan. Mayer FL; Whalen EA; Rheins LA J Toxicol Cutaneous Ocul Toxicol; 1994; 13(1):3-22. PubMed ID: 11659896 [No Abstract] [Full Text] [Related]
10. International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) adopts Consolidated Guideline on Good Clinical Practice in the Conduct of Clinical Trials on Medicinal Products for Human Use. Int Dig Health Legis; 1997; 48(2):231-4. PubMed ID: 11656783 [No Abstract] [Full Text] [Related]
11. European drug industry concerned over proposed clinical-trial legislation. Rogers A Lancet; 1997 Nov; 350(9091):1609. PubMed ID: 11655209 [No Abstract] [Full Text] [Related]
12. Trends in gene therapy regulation. Lecomte V; Taylor A Gene Ther; 1997 Feb; 4(2):77-8. PubMed ID: 11644906 [No Abstract] [Full Text] [Related]
13. Sharing scientific data II: normative issues. Weil V; Hollander R IRB; 1990; 12(2):7-8. PubMed ID: 11650369 [No Abstract] [Full Text] [Related]
14. European guidance on medical research. Council of Europe. Committee of Ministers Bull Med Ethics; 1990 Mar; No. 56():8-10. PubMed ID: 11650345 [No Abstract] [Full Text] [Related]
15. Whistleblowing in biomedical research: report from a workshop. Mishkin B IRB; 1982 Feb; 4(2):8-9. PubMed ID: 11658314 [No Abstract] [Full Text] [Related]
16. The development of regulatory standards for gene therapy in the European Union. De Jager CF Fordham Int Law J; 1995 Apr; 18(4):1303-39. PubMed ID: 11657449 [No Abstract] [Full Text] [Related]
17. Responses to the Gagnon report and REBs. Gagnon D; NCBHR Commun; 1993; 4(2):3-5. PubMed ID: 11652886 [No Abstract] [Full Text] [Related]
18. Europe says no to "FDA" but yes to bioethics. Rogers A Lancet; 1996 Nov; 348(9039):1441. PubMed ID: 11654447 [No Abstract] [Full Text] [Related]
19. Recommendation No. R (97) 5 of the Committee of Ministers to member states on the protection of medical data. Council of Europe Int Dig Health Legis; 1998; 49(3):502-8. PubMed ID: 11657540 [No Abstract] [Full Text] [Related]
20. French, European, and international legislation on bioethics. Leonir N Suffolk Univ Law Rev; 1993; 27(4):1249-70. PubMed ID: 11657038 [No Abstract] [Full Text] [Related] [Next] [New Search]