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Category: Informed Consent

Quality-Improvement Research and Informed Consent

  By admin Archives, Clinical Trials, Informed Consent

Franklin G. Miller, Ezekiel J. Emanuel | The New England Journal of Medicine | 21 Feb 2008 Tens of thousands of patients die each year because of hospitals’ failure to adhere consistently to standard procedures of safe and effective medical care.… Continue reading

Informed consent in Ghana: what do participants really understand?

  By admin Archives, Clinical Trials, Informed Consent

Hill Z., Tawiah-Agyemang C., Odei-Danso S., Kirkwood B. | Journal of Medical Ethics | 2008 | NCBI-PubMed ABSTRACT OBJECTIVES: To explore how subjects in a placebo-controlled vitamin A supplementation trial among Ghanaian women aged 15-45 years perceive the trial and… Continue reading

Interventions to improve research participant’s understanding in informed consent for research: A systematic review

  By admin Clinical Trials, Informed Consent

Flory, J., & Emanuel, E. | JAMA | 6 October 2004 | Vol. 292, No. 13 | Aim of article: To review research on interventions to improve research participants understanding of information disclosed in the informed consent process Read original… Continue reading

Seeking informed consent to cancer clinical trials: describing current practice

  By admin Archives, Clinical Trials, Informed Consent

Brown R. F., Butow P. N., Ellis P., Boyle F., Tattersall M. H. | Social Science and Medicine | June 2004 | NCBI-PubMed Abstract Clinical trials have come to be regarded as the gold standard for treatment evaluation. However, many… Continue reading

What makes clinical research in developing countries ethical? The benchmarks of ethical research

  By admin Archives, Clinical Trials, Informed Consent

Eamnuel E. J., Wendler D., Killen J., Grady C. | The Journal of Infectious Diseases | Vol. 189, Issue 5 | Oxford Journals | 1 March 2004 In recent years, there has been substantial debate about the ethics of research… Continue reading

Cancer clinical trial recruitment: The emerging role and perspectives of clinical research associates and data managers

  By admin Archives, Clinical Trials, Informed Consent

Martin Tattersall | Cancer | American Cancer Society | Volume 95, Issue 7, pages 1397–1400 | 1 October 2002 Clinical trials are an essential component of modern health care. The results of randomized clinical trials increasingly define current standards of care.… Continue reading

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    • Webinar on Intersectionality and Equity in Intellectual Property Rights in Healthcare
    • जेन्डर आधारित हिंसा (GBV) के मुद्दे पर कार्यशाला
  • What’s New

    • Dignity in death or discrimination in death?
    • Exploring Intellectual Property and Access to Medicines from a Gender Approach
    • Short course: GBV & Health systems roles and accountability
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    • The Unravelling Pandemic: Summary of the Intersectional Feminist Framework
  • Training, Building Capacities and Leadership

    Our Trainings and Capacity Building activities facilitate mobilization and provide support towards organizing around health issues and promoting health rights. They contribute to … Read more »

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    Research is an integral component of Sama’s work. Research is carried out on issues that the organization is already advocating around or in situations where we feel that there is a need to initiate … Read more »

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    Sama recognizes the critical role of advocacy in building collective understanding on various issues and to strengthen and sustain campaigns around them. Advocacy initiatives of Sama, including … Read more »

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    Sama undertakes Creation of Knowledge Resources and their Dissemination on different issues pertaining to women and health. This forms our core strategy on various issues and initiatives that Sama … Read more »

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