Contemporary requirements for organization ofclinical trials in health care system

Abstract


Clinical and population research is an important part of health care improvement and development. Quality and coordination as well as integration in medical practice are among priorities in modern research agenda. The article discusses modern approaches to design, quality and ethical issues in health care research.

About the authors

N. V. Vartapetova

Email: nvart@jsi.ru <mailto:nvart@jsi.ru>

A. V. Karpushkina

Email: nvart@jsi.ru <mailto:nvart@jsi.ru>

N. V. Vartepova

A. V. Karpushkina

References

  1. Комиссия Минздравсоцразвития России по разработке концепции развития здравоохранения до 2020 г. http://www.zdravo2020.ru/
  2. CONSORT, which stands for Consolidated Standards of Reporting Trials http://www.consort-statement.org/about-consort/the-consort-group/current-consort-group.
  3. Embedding Health Research. National Institute for Health Research Annual Report 2009/10. <http://www.nihr.ac.uk/Pages/default.aspx>
  4. Good Medical Practice - Guidance for Doctors. General Medical Council, 2006 <http://www.gmc-uk.org/static/documents/content/GMC_GMP_0911.pdf
  5. <http://obrnadzor.gov.ru/ru/docs/documents/>
  6. <http://clinicaltrials.gov/>
  7. <http://www.controlled-trials.com/>
  8. <http://www.who.int/ictrp/en/>
  9. R.H.Friis, T.A.Sellers. Epidemiology for public health practice. Jones and Bartlett Publishers, 2009.
  10. Steinbrook R. Public registration of clinical trials. New England Journal of Medicine, 2004, 351:315-317.
  11. TheResearchAssistant. Formulating a Research Question <http://>www.theresearchassistant.com/tutorial/2.asp

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Copyright (c) 2011 Vartapetova N.V., Karpushkina A.V., Vartepova N.V., Karpushkina A.V.

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This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.

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