{"id":11262,"date":"2023-06-26T11:21:37","date_gmt":"2023-06-26T03:21:37","guid":{"rendered":"https:\/\/medicine.nus.edu.sg\/cbme\/?page_id=11262"},"modified":"2023-11-07T15:55:13","modified_gmt":"2023-11-07T07:55:13","slug":"research-ethics-webinar-series","status":"publish","type":"page","link":"https:\/\/medicine.nus.edu.sg\/cbme\/research-ethics-webinar-series\/","title":{"rendered":"Research Ethics Webinar Series"},"content":{"rendered":"\t\t
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Series Summary<\/h4>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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There is wide recognition that responsible human subjects research requires careful consideration of a number of ethical issues, including balancing risks and benefits, avoiding exploitation, and promoting scientifically valuable research. IRBs are designed to assess these and other issues before research is conducted. However, like all governance systems, IRB review and other oversight mechanisms do not always conform to the ideals. IRBs can sometimes be too lenient, allowing research to go through that is ethically problematic; or, IRBs can be too strict, imposing requirements and delaying research conduct without good justification.<\/p>\n

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This webinar series consists of four sessions and will explore, through a deep-dive into four specific topics in research ethics, how IRBs and the research enterprise can best achieve this balance. The series will consist of talks by experts at the National University of Singapore\u2019s Centre for Biomedical Ethics, followed by an open Q&A for participants to broaden the discussion.<\/p>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t

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Speakers<\/h4>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Dr G. Owen Schaefer<\/a><\/h6>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Assistant Professor<\/p>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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CBmE, NUS<\/p>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t

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Professor Jerry Menikoff<\/a><\/h6>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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CBmE, NUS<\/p>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t

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Professor Julian Savulescu<\/a><\/h6>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Director<\/p>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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CBmE, NUS<\/p>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t

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Dr Sumytra Menon<\/a><\/h6>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Deputy Director<\/p>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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CBmE, NUS<\/p>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t

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Who should attend<\/h4>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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IRB members\/secretariat, researchers, clinician-scientists, and others involved in oversight\/regulation of research<\/u5:p><\/p>\n<\/div>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t

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Delivery Mode<\/h4>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Webinar via Zoom<\/p>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t

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Session Duration<\/h4>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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1 hour\u00a0<\/p>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t

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Session Dates & Time<\/h4>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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16 Aug, 30 Aug, 13 Sep & 27 Sep 2023, 12.00pm-1.00pm<\/p>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t

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There is no registration fee<\/p>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t

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Note: This Webinar\nseries concluded in September 2023. However, you can peruse the recordings of\nthe sessions via the links below.<\/span>
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What Counts as Research?<\/h4>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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What is and is not research has substantial implications for ethical conduct as well as regulatory compliance. In this session, we will summarize Singaporean standards concerning what is and is not research, with implications for what does and does not require IRB review. Along the way, we will also address the question of what do to in \u2018ambiguous\u2019 cases, where a project may straddle the research-practice or research-QI divide. This discussion will be enriched by discussion of cases drawn from actual experience of stakeholders.<\/span><\/p>\n

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    Risks in Research<\/h4>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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    Assessing risks of a study is one of the central tasks of IRBs in protecting participants. This session will outline the notion of risks, the distinction between study and standard-of-care risks, and the special category of \u2018minimal risks\u2019.<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

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      IRBs in Singapore and elsewhere are given scope to review all aspects of study design, and often give comments related to scientific matters such as articulation of aims and sample size calculation. This session will outline why scientific validity is properly a part of IRB review. Understanding the purpose of such review will also help shed light on its limitations \u2013 where the IRB can reasonably insist on changes, and where deferment to researchers is appropriate.<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

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        Coercion, Incentives and Inducement <\/h4>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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        by Professor Jerry Menikoff <\/h6>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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        and Dr Sumytra Menon<\/h6>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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        In Singapore, there is limited national guidance on payment to research participants, leaving considerable IRB and researcher discretion. This session will outline the general ethical debate surrounding incentives and \u2018undue inducement\u2019. In particular, recent developments in the international literature will be highlighted that have put pressure on the notion that overpayment is a serious ethical concern.<\/span><\/p>\n

        <\/p>\n

          <\/ol>\n

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          <\/div>\n\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<\/div>\n\t\t","protected":false},"excerpt":{"rendered":"

          Series Summary There is wide recognition that responsible human subjects research requires careful consideration of a number of ethical issues,…<\/p>\n","protected":false},"author":8998,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-11262","page","type-page","status-publish","hentry"],"acf":[],"yoast_head":"\nResearch Ethics Webinar Series - Centre for Biomedical Ethics \u2013 School of Medicine, National University of Singapore - CBmE<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/medicine.nus.edu.sg\/cbme\/research-ethics-webinar-series\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Research Ethics Webinar Series - Centre for Biomedical Ethics \u2013 School of Medicine, National University of Singapore - 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