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Original Article

WHO Guidelines for Good Clinical Practice (GCP) for Trials on Pharmaceutical Products: Responsibilities of the Investigator

Pages 89-94 | Published online: 08 Jul 2009

References

  • Who. Basic Documents: Constitution. WHO, Geneva 1990
  • Idänpään‐Helkkilä J E. Role of WHO in harmonization of requirements for pharmaceutical products. Proceedings of the First International Conference on Harmonization, Brussels, 1991, P F D'Arcy, D WG Harron. 1992; 27–8, Published by the Queen's University of Belfast (ISBN 0 85389 4310)
  • Council for International Organizations of Medical Sciences (CIOMS). The International Ethical Guidelines for Biomedical Research Involving Human Subjects. Geneva 1993
  • WHO. Proposed WHO Guidelines for Good Clinical Practice (GCP) for Trials on Pharmaceutical Products. WHO Drug Information 1992; 6: 170

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