Ethics-related Legal Amendments and Ethics Applications for Medical Research
Laws and guidelines relating to ethics are now being issued by the government nearly every year. Not only do dental professionals conducting clinical research have to comply with an increasing number of regulations ; they must first gather a large amount of information to store as knowledge. Since t...
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Published in | Journal of Japanese Society of Oral Implantology Vol. 32; no. 4; pp. 265 - 274 |
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Main Authors | , |
Format | Journal Article |
Language | Japanese |
Published |
Japanese Society of Oral Implantology
31.12.2019
公益社団法人 日本口腔インプラント学会 |
Subjects | |
Online Access | Get full text |
ISSN | 0914-6695 2187-9117 |
DOI | 10.11237/jsoi.32.265 |
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Abstract | Laws and guidelines relating to ethics are now being issued by the government nearly every year. Not only do dental professionals conducting clinical research have to comply with an increasing number of regulations ; they must first gather a large amount of information to store as knowledge. Since the scope of application of the "Ethics Guidelines for Epidemiological Research" (revised in 2007) and the "Ethical Guidelines for Clinical Research" (revised in 2008)─both issued by the Ministry of Health, Labour and Welfare and the Ministry of Education, Culture, Sports, Science and Technology─was considered difficult to interpret, the guidelines were integrated into the "Ethical Guidelines for Medical and Health Research Involving Human Subjects," which have been in effect since 2015. Following their enforcement, with the recent full-fledged implementation of the updated Act on the Protection of Personal Information, which clarifies the scope of personal information and provides for its legitimate distribution, these guidelines have also been revised to ensure proper handling of personal information in research, and came into effect on May 30, 2017. In recent years, several such new or revised ethical laws and guidelines have been implemented. Obviously, non-compliance is not an option, so a realistic outlook of the facts is necessary to prevent researchers from abandoning research in dejection. It is therefore essential to grasp the background of the strengthened regulations and understand their purpose and requirements. An ethics training conference known as the "Ethics Committee Seminar," hosted by the Japanese Society of Oral Implantology, was relaunched as the "Ethics Seminar on Medical Research" in response to the overwhelmingly rapid revision of guidelines and to attempt to disseminate information. In addition to imparting an understanding of the original ethical guidelines, the announced purpose of this seminar is to explain what kind of research requires an ethics review in this academic society and, for research and case reports that require it, how to apply to the ethics review committee. However, because of the large number of members, it is difficult to provide ethics review training to everyone. Since members still perceive a lack of clarity in ethics applications, this article explains the essence of medical ethics and provides commentary on details of the latest amendments in ethics regulations, as well as ways of creating research ethics applications to help members understand what kind of academic research requires an ethics review. |
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AbstractList | Laws and guidelines relating to ethics are now being issued by the government nearly every year. Not only do dental professionals conducting clinical research have to comply with an increasing number of regulations ; they must first gather a large amount of information to store as knowledge. Since the scope of application of the "Ethics Guidelines for Epidemiological Research" (revised in 2007) and the "Ethical Guidelines for Clinical Research" (revised in 2008)─both issued by the Ministry of Health, Labour and Welfare and the Ministry of Education, Culture, Sports, Science and Technology─was considered difficult to interpret, the guidelines were integrated into the "Ethical Guidelines for Medical and Health Research Involving Human Subjects," which have been in effect since 2015. Following their enforcement, with the recent full-fledged implementation of the updated Act on the Protection of Personal Information, which clarifies the scope of personal information and provides for its legitimate distribution, these guidelines have also been revised to ensure proper handling of personal information in research, and came into effect on May 30, 2017. In recent years, several such new or revised ethical laws and guidelines have been implemented. Obviously, non-compliance is not an option, so a realistic outlook of the facts is necessary to prevent researchers from abandoning research in dejection. It is therefore essential to grasp the background of the strengthened regulations and understand their purpose and requirements. An ethics training conference known as the "Ethics Committee Seminar," hosted by the Japanese Society of Oral Implantology, was relaunched as the "Ethics Seminar on Medical Research" in response to the overwhelmingly rapid revision of guidelines and to attempt to disseminate information. In addition to imparting an understanding of the original ethical guidelines, the announced purpose of this seminar is to explain what kind of research requires an ethics review in this academic society and, for research and case reports that require it, how to apply to the ethics review committee. However, because of the large number of members, it is difficult to provide ethics review training to everyone. Since members still perceive a lack of clarity in ethics applications, this article explains the essence of medical ethics and provides commentary on details of the latest amendments in ethics regulations, as well as ways of creating research ethics applications to help members understand what kind of academic research requires an ethics review. Laws and guidelines relating to ethics are now being issued by the government nearly every year. Not only do dental professionals conducting clinical research have to comply with an increasing number of regulations ; they must first gather a large amount of information to store as knowledge. Since the scope of application of the “Ethics Guidelines for Epidemiological Research” (revised in 2007) and the “Ethical Guidelines for Clinical Research” (revised in 2008)─both issued by the Ministry of Health, Labour and Welfare and the Ministry of Education, Culture, Sports, Science and Technology─was considered difficult to interpret, the guidelines were integrated into the “Ethical Guidelines for Medical and Health Research Involving Human Subjects,” which have been in effect since 2015. Following their enforcement, with the recent full-fledged implementation of the updated Act on the Protection of Personal Information, which clarifies the scope of personal information and provides for its legitimate distribution, these guidelines have also been revised to ensure proper handling of personal information in research, and came into effect on May 30, 2017. In recent years, several such new or revised ethical laws and guidelines have been implemented. Obviously, non-compliance is not an option, so a realistic outlook of the facts is necessary to prevent researchers from abandoning research in dejection. It is therefore essential to grasp the background of the strengthened regulations and understand their purpose and requirements. An ethics training conference known as the “Ethics Committee Seminar,” hosted by the Japanese Society of Oral Implantology, was relaunched as the “Ethics Seminar on Medical Research” in response to the overwhelmingly rapid revision of guidelines and to attempt to disseminate information. In addition to imparting an understanding of the original ethical guidelines, the announced purpose of this seminar is to explain what kind of research requires an ethics review in this academic society and, for research and case reports that require it, how to apply to the ethics review committee. However, because of the large number of members, it is difficult to provide ethics review training to everyone. Since members still perceive a lack of clarity in ethics applications, this article explains the essence of medical ethics and provides commentary on details of the latest amendments in ethics regulations, as well as ways of creating research ethics applications to help members understand what kind of academic research requires an ethics review. 行政からの倫理にかかわる法律や指針が,毎年のように発出されてきている.2007年改正の「疫学研究に関する倫理指針」と,2008年改正の「臨床研究に関する倫理指針」を母体に,これらの指針を統合した「人を対象とする医学系研究に関する倫理指針」,いわゆる医学系研究指針が2015年より施行されてきた.その後,さらに個人情報保護法の全面施行によりこの医学系研究指針も改正され,2017年5月30日に施行されるにいたっている.当然,法令遵守は避けては通れない道であるから,この事実を悲観して研究から遠ざかることのないようにしなければならない.そのためには規制が強化された背景を理解し,何が求められ,何をしなければいけないのかを把握しておくことはたいへん重要である.目まぐるしく改正される指針に対応するために,また本学会員に対して周知徹底するために,学術大会において「医学系研究に関する倫理セミナー」を開催してきた.本稿では,本学会員から倫理申請にあたって,いまだに不明点があるというご意見を背景に,医療倫理の本質を解説するとともに,倫理審査が必要な学会発表の内容を理解していただくために,最新の倫理関連法令の改定内容と本学会における研究倫理の申請方法について解説する. |
Author | TODA, Isumi BABA, Shunsuke |
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References_xml | – reference: 8) 山本一世.歯科審美学.日本歯科審美学会編.歯科審美学,京都:永末書店,166-171.2019. – reference: 11) 厚生労働省.医業若しくは歯科医業又は病院若しくは診療所に関する広告等に関する指針(医療広告ガイドライン).厚生労働省. https://www.mhlw.go.jp/file/06-Seisakujouhou-10800000-Iseikyoku/0000209841.pdf (参照2019-08-27) – reference: 5) 文部科学省,厚生労働省.人を対象とする医学系研究に関する倫理指針.文部科学省,厚生労働省. https://www.mhlw.go.jp/file/06-Seisakujouhou-10600000-Daijinkanboukouseikagakuka/0000153339.pdf (参照2019-08-26) – reference: 10) 厚生労働省.臨床研究法について.厚生労働省. https://www.mhlw.go.jp/stf/seisakunitsuite/bunya/0000163417.html (参照2019-08-27) – reference: 3) 後藤昌昭,若松陽子.デンタルインプラントの研究に関係する倫理問題と対応.日口腔インプラント誌 2012;25:693-698. – reference: 2) 厚生労働省.医薬品,医療機器等の品質,有効性及び安全性の確保等に関する法律.e-Gov. https://elaws.e-gov.go.jp/search/elawsSearch/elaws_search/lsg0500/detail?lawId=335AC0000000145 (参照2019-08-26) – reference: 4) 厚生労働省.再生医療等の安全性の確保等に関する法律について.厚生労働省. https://www.mhlw.go.jp/file/06-Seisakujouhou-10800000-Iseikyoku/0000079192.pdf (参照2019-08-26) – reference: 13) 文部科学省,厚生労働省.人を対象とする医学系研究に関する倫理指針ガイダンス.文部科学省,厚生労働省. https://www.mhlw.go.jp/file/06-Seisakujouhou-10600000-Daijinkanboukouseikagakuka/0000166072.pdf (参照2019-08-26) – reference: 6) 文部科学省,厚生労働省,経済産業省.個人情報保護法等の改正に伴う研究倫理指針の改正について.文部科学省,厚生労働省,経済産業省. https://www.mhlw.go.jp/file/06-Seisakujouhou-10600000-Daijinkanboukouseikagakuka/0000170955.pdf (参照2019-08-26) – reference: 12) 日本口腔インプラント学会.日本口腔インプラント学会指定研修施設(臨床系).日本口腔インプラント学会. http://www.shika-implant.org/list/clinical.html (参照2019-08-27) – reference: 9) 厚生労働省医薬・生活衛生局長.未承認医療機器の展示会等への出展について.厚生労働省. https://kouseikyoku.mhlw.go.jp/kinki/gyomu/gyomu/yakkan/documents/20170609yn060901.pdf#search=%27%E5%AD%A6%E4%BC%9A%E5%B1%95%E7%A4%BA%E3%81%AB%E9%96%A2%E3%81%99%E3%82%8B%E3%82%AC%E3%82%A4%E3%83%89%E3%83%A9%E3%82%A4%E3%83%B3%27 (参照2019-08-26) – reference: 1) 日本医師会.ヘルシンキ宣言.日本医師会. http://www.med.or.jp/wma/helsinki.html (参照2019-08-26) – reference: 7) 個人情報保護委員会.個人情報保護法ハンドブック.個人情報保護委員会. https://www.ppc.go.jp/files/pdf/kojinjouhou_handbook.pdf (参照2019-08-26) |
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SubjectTerms | advertising regulations ethics review medical ethics research ethics 倫理審査 医療倫理 広告規制 研究倫理 |
Title | Ethics-related Legal Amendments and Ethics Applications for Medical Research |
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