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Organization of the Trial attheInvestigator Site

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Part of the book series: Clinical Trials ((CLINICAL))

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References

  1. Information for Sponsor-Investigators Submitting Investigational New Drug Applications (INDs). US Food and Drug Administration. Available at http://www.fda.gov/cder/forms/1571–1572-help.html.

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  2. ICH Harmonised Tripartite Guideline for Good Clinical Practice E6(R1). International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use. Available at www.ich.org/cache/compo/276–254-1.html

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  3. World Medical Association Declaration of Helsinki. Ethical Principles for Medical Research Involving Human Subjects. Available at http://www.wma.net/e/policy/b3.htm.

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  4. United Kingdom Central Council for Nursing, Midwifery and Health Visiting. Code of professional conduct for the nurse, midwife and health visitor. London: UKCC; 1992.

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© 2008 Springer-Verlag London Limited

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Shotton, J., Reid, D.M., Miller, C.G. (2008). Organization of the Trial attheInvestigator Site. In: Reid, D.M., Miller, C.G. (eds) Clinical Trials in Rheumatoid Arthritis and Osteoarthritis. Clinical Trials. Springer, London. https://doi.org/10.1007/978-1-84628-742-8_9

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  • DOI: https://doi.org/10.1007/978-1-84628-742-8_9

  • Publisher Name: Springer, London

  • Print ISBN: 978-1-85233-874-9

  • Online ISBN: 978-1-84628-742-8

  • eBook Packages: MedicineMedicine (R0)

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