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).
Author information
Authors and Affiliations
Additional information
An earlier journalistic version of this meeting report appeared in Pharmaceutical Physician.
Rights and permissions
About this article
Cite this article
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
Published:
Issue Date:
DOI: https://doi.org/10.2165/00124363-200204000-00007