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1.
J Med Ethics ; 44(10): 710-716, 2018 10.
Artigo em Inglês | MEDLINE | ID: mdl-29018176

RESUMO

There is a growing body of literature that has sought to undermine systems of ethical regulation, and governance more generally, within the social sciences. In this paper, we argue that any general claim for a system of research ethics governance in social research depends on clarifying the nature of the stake that society has in research. We show that certain accounts of this stake-protecting researchers' freedoms; ensuring accountability for resources; safeguarding welfare; and supporting democracy-raise relevant ethical considerations that are reasonably contested. However, these accounts cannot underpin a general claim in favour of, or against, a system of research ethics governance. Instead, we defend governance in social research on the grounds that research, as an institutionalised form of enquiry, is a constitutive element of human flourishing, and that society ought to be concerned with the flourishing of its members. We conclude by considering the governance arrangements that follow from, and are justified by, our arguments.


Assuntos
Pesquisa Biomédica/ética , Comitês de Ética em Pesquisa/ética , Ética em Pesquisa , Pesquisa Biomédica/legislação & jurisprudência , Comitês de Ética em Pesquisa/legislação & jurisprudência , Governo , Humanos , Justiça Social
2.
Soc Stud Sci ; 53(3): 315-340, 2023 06.
Artigo em Inglês | MEDLINE | ID: mdl-36802925

RESUMO

The 2012 Menlo Report was an effort in which a group of computer scientists, US government funders, and lawyers produced ethics guidelines for research in information and communications technology (ICT). Here we study Menlo as a case of what we call ethics governance in the making, finding that this process examines past controversies and enrols existing networks to connect the everyday practice of ethics with ethics as a form of governance. To create the Menlo Report, authors and funders relied on bricolage work with existing, available resources, which significantly shaped both the report's contents and impacts. Report authors were motivated by both forward- and backward-looking goals: enabling new data-sharing as well as addressing past controversies and their implications for the field's body of research. Authors also grappled with uncertainty about which ethical frameworks were appropriate and made the decision to classify much network data as human subjects data. Finally, the Menlo Report authors attempted to enrol multiple existing networks in governance through appeals to local research communities as well as taking steps towards federal rulemaking. The Menlo Report serves as a case study in how to study ethics governance in the making: with attention to resources, adaptation, and bricolage, and with a focus on both the uncertainties the process tries to repair, as well as the new uncertainties the process uncovers, which will become the site of future ethics work.


Assuntos
Comitês de Ética em Pesquisa , Governo , Humanos , Tecnologia da Informação
3.
Front Pharmacol ; 14: 1214590, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-37701030

RESUMO

As international academic exchanges and cooperation deepen, China has actively engaged in international biomedical research collaboration and achieved significant success. However, these accomplishments have been accompanied by ethical controversies and issues, with ethics dumping being a recurrently discussed focus among scholars. This paper reviews ethics dumping incidents in China's biomedical research field and analyzes the underlying causes to answer why China is often susceptible to ethics dumping. We argue that the primary reasons include weak ethical awareness among some researchers, an oversimplified research evaluation system, gaps in relevant ethics governance and oversight mechanisms, and limited capabilities of certain ethics committees. To address these issues, we propose five ethics governance recommendations: establishing refined ethics committees at various levels and types; advancing theoretical and practical research on science and technology ethics governance; strengthening legislation and regulation related to emerging science and technology; emphasizing self-regulation and capacity building of research institutions; and providing special protection and healthcare for victims of ethics dumping. The aim is to enhance China's research supervision system and prevent similar ethics dumping incidents from recurring.

4.
Chinese Medical Ethics ; (6): 597-605, 2023.
Artigo em Zh | WPRIM | ID: wpr-1005676

RESUMO

The healthy development of science and technology (Sci. & Tech) innovation is inseparable from Sci. & Tech ethics. The innovation subject is the driving force of Sci. & Tech innovation. The improvement of Sci. & Tech ethical management ability is conducive to improving the China’s Sci. & Tech ethics governance system. Therefore, this paper deeply analyzed the current status of Sci. & Tech ethics management of the 76 innovation subjects from five aspects, and found that the construction of Sci. & Tech ethics management of Chinese innovation subjects has achieved initial results, but there was still room for further improvement. Based on the problems existing in the Sci. & Tech ethics management of innovation subjects, this paper proposed six strategic suggestions that strengthening the construction and research of artificial intelligence ethics management systems, establishing and improving ethics committees and management systems, actively implementing the registration of Sci. & Tech ethics management information, regularly organizing and participating in various forms of Sci. & Tech ethics training, attaching importance to the reserve and cultivation of composite Sci. & Tech ethics management talents, and cooperating to establish a Sci. & Tech ethics case library, with a view to enhancing the Sci. & Tech ethics management ability of Chinese innovation subjects to adapt to the needs of the healthy development of Sci. & Tech in China.

5.
Rev. bioét. derecho ; (58): 109-127, Jul. 2023.
Artigo em Espanhol | IBECS (Espanha) | ID: ibc-222831

RESUMO

En la última década, el Paraguay ha presentado avances en el desarrollo de la investigación relacionada con la salud con seres humanos.Sin embargo, existe una obligación estatal de asegurar que las investigaciones sean realizadas éticamente: protegiendo la dignidad, los derechos y el bienestar de los participantes, la integridad científica y la adherencia a pautas éticas locales e internacionales. Los comités de ética de la investigación institucionales constituyen la instancia o recurso principal para garantizar la mencionada obligación. Ante lo expuesto y el contexto carente de adecuada regulación en el cual actualmente se desarrollan las investigaciones en el país, en el presente artículo defenderemos el imperativo ético de establecer un sistema de acreditación de los comités de ética de la investigación. Para ello, expondremos y justificaremos su necesidad y buscaremos responder algunas objeciones relativas al imperativo ético defendido, como, por ejemplo, el valor per se de la acreditación de los comités de ética en investigación en la protección de los participantes, la inversión de tiempo y burocracia que implican los procesos de acreditación y el marco regulatorio incipiente para las investigaciones en seres humanos en el Paraguay. Finalmente, propondremos el fortalecimiento de la gobernanza de la ética de la investigación en el país, como medio principal para establecer, implementar y supervisar un sistema de acreditación de los comités de ética de la investigación.(AU)


A l'última dècada, el Paraguai ha presentat avençosen el desenvolupament de la recerca relacionada amb la salut amb éssers humans. Tot i això, hi ha una obligació estatal d'assegurar que les investigacions siguin realitzades èticament: protegint la dignitat, els drets i el benestar dels participants, la integritat científica i l'adherència a pautes ètiques locals i internacionals. Els comitès d'ètica de la investigació institucionals constitueixen la instància o el recurs principal per garantir l'obligació esmentada. Davant del que s'ha exposat i el context sense regulació adequada en el qual actualment es desenvolupen les investigacions al país, en aquest article defensarem l'imperatiu ètic d'establir un sistema d'acreditació dels comitès d'ètica de la investigació. Per això, exposarem i justificarem la seva necessitat i buscarem respondre algunes objeccions relatives a l'imperatiu ètic defensat, com, per exemple, el valor perseguit de l'acreditació dels comitès d'ètica en recerca en la protecció dels participants, la inversió de temps i burocràcia que impliquen els processos d'acreditació i el marc regulador incipient per a les investigacions en éssers humans al Paraguai. Finalment, proposarem l'enfortiment de la governança de l'ètica de la investigació al país com a mitjà principal per establir, implementar i supervisar un sistema d'acreditació dels comitès d'ètica de la investigació.(AU)


In the last decade, Paraguay has made progress in the development of health-related research involving human subjects. This entails the obligation of the State to ensure that research is conducted ethically: protecting the dignity, rights and welfare of the participants, scientific integrity and adherence to international ethical guidelines. Research Ethics Committees are the main instance or resource to guarantee the aforementioned obligation. In view of the above and the context lacking adequate regulation in which research is currently carried out in the country, this article will defend the ethical imperative of establishing an accreditation system for research ethics committees. To this end, its necessity will be presented and justified and some objections related to the ethical imperative defended will be answered, such as the per se value of the accreditation of research ethics committees in the protection of participants, the investment of time and bureaucracy involved in the accreditation processes and the incipient regulatory framework for research on human beings in Paraguay. Finally, it will be proposed to strengthen the governance of research ethics in the country, as the main means to establish, implement and supervise an accreditation system for research ethics committees.(AU)


Assuntos
Humanos , Comitês de Ética em Pesquisa , Humanos , Temas Bioéticos , Pesquisa Científica e Desenvolvimento Tecnológico , Paraguai , Bioética , Pesquisa
6.
Artigo em Zh | WPRIM | ID: wpr-958691

RESUMO

Objective:Through text mining, to clarify the change characteristics and evolution patterns of China's scientific research integrity policies, thereby providing a reference basis for the formulation and implementation of medical scientific research integrity governance policies.Methods:Using cost-CM6 and SPSS software, co-word analysis, social semantic network, and cluster analysis methods, data mining was conducted on 297 national scientific research integrity policy texts from 2002 to 2021.Results:China′s research integrity policies have experienced three development stages: academic ethics construction period(2002-2008), research integrity construction period(2009-2015), and academic environment optimization period(2016-2021), with the rapid development of both quantity and quality of policies, gradual clarification of rules for investigation and handling of research integrity cases, continuous improvement of accountability mechanism, and more powerful disciplinary measures for dishonesty. The construction of scientific research integrity formed a joint force pattern under the leadership of the central government and coordinated governance of multiple departments. Research misconduct incidents and public concern accelerated the improvement of the scientific research credibility policy system. Adhere to" no exclusion zone, full coverage, zero tolerance" has become the work guide of scientific research integrity governance.Conclusions:It is suggested to continuously improve the effectiveness of medical research integrity governance by strengthening medical integrity education and enhancing self-discipline consciousness, improving supervision mechanisms, strengthening process management and plagiarism checking of medical achievements, and adopting a two-pronged approach of " severe punishment" and " good governance" .

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