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Category: Archives

US woman blessed with Mumbai miracle

  By admin December 4, 2009 April 2, 2016 Archives, Assisted Reproductive Technologies, Surrogacy

Pratibha Masand | The Times of India | Mumbai | 4 December 2009 When the US-resident Joy (38) held her baby Samuel for the first time at Mumbai’s Lilawati Hospital on November 24, a mixture of emotions flooded her heart.… Continue reading

German or Indian? Surrogate twins in legal no-man’s land

  By admin December 1, 2009 April 2, 2016 Archives, Assisted Reproductive Technologies, Surrogacy

Dhananjay Mahapatra | The Times of India | New Delhi | 1 December 2009 A childless German couple who had twins through a Gujarati surrogate mother are negotiating their first challenge as parents, in the Supreme Court — German laws… Continue reading

Surfing for surrogates

  By admin October 7, 2009 April 2, 2016 Archives, Assisted Reproductive Technologies, Surrogacy

John Stock | The Week | 7 October 2009 A couple desperately seek a surrogate mother to have a child. Nikki and Bobby Bains have tried everything to have a child. They have undergone five expensive in vitro fertilisation treatments,… Continue reading

Fatal trials: clinical trials are killing people

  By admin September 27, 2009 April 27, 2016 Archives, Clinical Trials, Compensation

Amit Sengupta | Indian Journal of Medical Ethics | Vol 6, No. 3 | 2009 In many quarters there is satisfaction that India is developing into the “clinical trials capital” of the globe. By all accounts the business of conducting… Continue reading

Benefits and Burdens of Participation in a Longitudinal Clinical Trial

  By admin September 18, 2009 April 8, 2016 Archives, Clinical Trials, Compensation

Jaime Lazovski, Marcelo Losso, Benjamin Krohmal, Ezekiel J. Emanuel, Christine Grady, David Wendler | Journal of Empirical Research on Human Research Ethics | September 2009 | Source: NCBI-PubMed Abstract Systematic data on the impact that longitudinal clinical trials have on… Continue reading

Evaluation of the ability of clinical research participants to comprehend informed consent form

  By admin September 17, 2009 April 7, 2016 Archives, Clinical Trials, Informed Consent

Bhansali S., Shafiq N., Malhotra S., Pandhi P., Singh I., Venkateshan S. P., Siddhu S., Sharma Y. P., Talwar K. K. | Contemporary Clinical Trials | 2009 | NCBI-PubMed | Abstract The comprehension of informed consent is an integral part… Continue reading

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  • What’s New

    • Mental Health and Sickle Cell Disease: What Policy Leaves Unseen
    • Zine Posters on Sickle Cell Disease
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    • Workshop on Integrating Disability and Psychosocial Support within Sickle Cell Disease Care
    • Session on GBV for the 16 Days of Activism 2025
    • Workshop in Raipur on SCD: Some Photographs
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    • Workshop: SCD-A Social & Gendered Issue and Perspectives
    • Roundtable on Psychosocial Health, Disability Justice and SCD: Some photographs
    • Amplifying Psychosocial Health and Disability Justice in the Realm of SCD: A follow-up roundtable
    • Addressing Sickle Cell Disease, Gender, and Disability Justice Interlinkages
  • 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 »

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