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Category: Clinical Trials

Clinical trials in India: ethical concerns

  By admin Archives, Bioethics, Clinical Trials

Patralekha Chatterjee | Bulletin of the World Health Organisation | Volume 86, Number 8 | August 2008 According to the Associated Chambers of Commerce and Industry, an influential national industry association, India is set to grab clinical trials business valued… Continue reading

What should research participants understand to understand they are participants in research?

  By admin Archives, Clinical Trials, Informed Consent

David Wendler, Christine Grady | Bioethics | Vol. 22, Issue 4 | 31 July 2008 To give valid informed consent to participate in clinical research, potential participants should understand the risks, potential benefits, procedures, and alternatives. Potential participants also should… Continue reading

Clinical research: protection of the “vulnerable”?

  By admin Archives, Bioethics, Clinical Trials

Park S. S., Grayson M. H. | PubMed | 2008 May;121(5):1103-7 In this age of evidence-based medicine, clinical research is critical for developing new therapeutics and determining the best way to use these therapies. To perform appropriate clinical research, researchers must… Continue reading

Informed Consent in Developing Countries: Myth or Reality?

  By admin Archives, Clinical Trials, Informed Consent

Ben Campbell | 2008 | Source: Dartmouth Ethics Institute | In the last decade, biomedical research conducted by researchers from developed countries in developing countries has been a topic of significant controversy. One serious concern is that research participants in… Continue reading

Initial experience with a group presentation of study results to research participants

  By admin Archives, Clinical Trials, Compensation

Andrew L avins, Stephen Bent, Amy Padula, Suzanne Staccone, Evelyn Badua, Harley Goldberg | BioMed Central | Trials | 21 March 2008 | Source: NCBI-PubMed Central Abstract Background Despite ethical imperatives, informing research participants about the results of the studies… Continue reading

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

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  • Building Capacities and Leadership

    Our training and capacity-building initiatives are designed to strengthen women’s and young people’s (especially young women and girls) leadership in rural and peri-urban … Read more »

  • Research

    Over the last 25 years, Sama – Resource Group for Women and Health has conducted research on wide-ranging issues related to women’s health, public health, mental health, gender-based violence (GBV), and sexual and reproductive … Read more »

  • Advocacy

    With our strong and expanding connections at both the policy and grassroots levels, we are well placed to shape policy initiatives that reflect ground realities. We also create platforms that support community … Read more »

  • Knowledge Creation

    The knowledge resources we create cover a broad range of formats, including research papers, essays, articles, podcasts, training modules, policy briefs, information guides, videos, booklets, and posters … Read more »

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