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Fraud and misconduct in biomedical research — 15 January 2002

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Further reading

  • Directive on the approximation of the laws, regulations and administrative provisions of the member states relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use (May 2001) EU Directive 2001/120/EC.

  • DH Research Governance Framework for Health and Social Care (March 2001) http://www.doh.gov.uk/research/rd3/nhsrandd/researchgovernance/govhome.htm

  • DH Governance arrangements for NHS Research Ethics Committees (July 2001) http://www.doh.gov.uk/research/rd1/researchgovernance/corec.htm

  • EC Draft additional protocol to the Convention on Human Rights and Biomedicine, on Biomedical Research. Consultation document Strasbourg (July 2001).

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An earlier journalistic version of this meeting report appeared in Pharmaceutical Physician.

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Boardman, H. Fraud and misconduct in biomedical research — 15 January 2002. International Journal of Pharmaceutical Medicine 16, 97–102 (2002). https://doi.org/10.2165/00124363-200204000-00007

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  • DOI: https://doi.org/10.2165/00124363-200204000-00007

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