305 results on '"Moodley, Keymanthri"'
Search Results
2. COVID-19 vaccines
3. Ethics and governance challenges related to genomic data sharing in southern Africa: the case of SARS-CoV-2
4. Data as scientific currency: Challenges experienced by researchers with sharing health data in sub-Saharan Africa.
5. Exploring views of South African research ethics committees on pandemic preparedness and response during COVID-19.
6. Trust as moral currency: Perspectives of health researchers in sub-Saharan Africa on strategies to promote equitable data sharing.
7. Cross-border data sharing through the lens of research ethics committee members in sub-Saharan Africa
8. Digital tools for youth health promotion: principles, policies and practices in sub-Saharan Africa
9. Liver transplantation for non-resectable colorectal liver metastases: the International Hepato-Pancreato-Biliary Association consensus guidelines
10. What Could “Fair Allocation” during the Covid-19 Crisis Possibly Mean in Sub-Saharan Africa?
11. Negotiating Requests for Reimbursement for Community Engagement : Challenges in Developing an Educational Video for Genomic Biobanking Research in South Africa
12. Awareness, experiences and perceptions regarding genetic testing and the return of genetic and genomics results in a hypothetical research context among patients in Uganda: a qualitative study
13. International AIDS Society global scientific strategy: towards an HIV cure 2016
14. COVID-19 underscores the important role of Clinical Ethics Committees in Africa
15. Vaccine inequity is unethical
16. A response to Thaldar et al. (2023): Data sharing governance in sub-Saharan Africa during public health emergencies
17. Taxonomy and ethical considerations of digital health promotion tools for youth: Selected examples from three Sub-Saharan African countries (Preprint)
18. Penile transplantation as an appropriate response to botched traditional circumcisions in South Africa : an argument against
19. Science, Race and Ethics
20. A framework for tiered informed consent for health genomic research in Africa
21. Clinical Ethics Committees in Africa: lost in the shadow of RECs/IRBs?
22. The many faces of the big data revolution in health for sub-Saharan Africa
23. Data sharing and data governance in sub-Saharan Africa: Perspectives from researchers and scientists engaged in data-intensive research
24. Public health research using cell phone derived mobility data in sub-Saharan Africa: Ethical issues
25. Exploring perspectives of research ethics committee members on the governance of big data in sub-Saharan Africa
26. Bioethics: Clinical
27. Standards of Care
28. The psychology of “cure” - unique challenges to consent processes in HIV cure research in South Africa
29. Legitimacy, Trust and Stakeholder Engagement: Biobanking in South Africa
30. Phase 3 Oncology Clinical Trials in South Africa : Experimentation or Therapeutic Misconception?
31. Ethical Concerns in Disaster Research—A South African Perspective
32. Results of a self-assessment tool to assess the operational characteristics of research ethics committees in low-and middle-income countries
33. Feedback of individual genetic and genomics research results: A qualitative study involving grassroots communities in Uganda
34. Data sharing governance in sub-Saharan Africa during public health emergencies: Gaps and guidance
35. Consensus standards for introductory e-learning courses in human participants research ethics
36. Rules of engagement: perspectives on stakeholder engagement for genomic biobanking research in South Africa
37. Disparate compensation policies for research related injury in an era of multinational trials: a case study of Brazil, Russia, India, China and South Africa
38. Research-Related Stakeholders' Perspectives on Sociocultural Considerations in Biobanking Practice in South Africa
39. Online Training as a Means to Improve the Understanding of Ethical, Legal, and Social Aspects of Biobanking Research: Stakeholder Perspectives from South Africa
40. Ethics, human rights and HIV vaccine trials in low-income settings
41. Electronic consent in a COVID-19 vaccine implementation trial in South Africa: Participant perspectives
42. The ethics behind mandatory COVID-19 vaccination post-Omicron: The South African context
43. Teaching Medical Ethics to Undergraduate Students in Post-Apartheid South Africa, 2003-2006
44. The acceptability of delayed consent for prehospital emergency care research in the Western Cape province of South Africa
45. Research-Related Stakeholders' Perspectives on Sociocultural Considerations in Biobanking Practice in South Africa.
46. Bioethics: Clinical
47. Standards of Care
48. Pandemics Remind Us of Our Responsibility to Ourselves, Others and Future Generations: A Time for Intergenerational Justice?
49. Medically Unnecessary Genital Cutting and the Rights of the Child: Moving Toward Consensus
50. Ethical considerations for vaccination, programmes in acute humanitarian emergencies/Considerations ethiques des programmes de vaccination dans les situations d'urgence humanitaire graves/ Consideraciones eticas para los programas de vacunacion en las emergencias humanitarias graves
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