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ICMEGR · Registering as Listener

International Conference on Medical Ethics and Genetic Research

11 - 12 Feb 2027 Ulaanbaatar, Mongolia Standard / Physical Participation
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$120
virtual · $135 in person
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Registration summary

ConferenceICMEGR
ModeStandard / Physical
ParticipationListener
Registration fee$135.00
Bank charges (5.8%)$7.83
Total payable$142.83
Includes all bank processing charges — the amount above is exactly what will be charged.

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• Conference Session Tracks •
SDGs
SDG-Aligned Research Themes

ICMEGR conference tracks support global knowledge exchange, innovation, and sustainable development priorities across diverse disciplines.

SDG 3 - Good Health and Well-being SDG 10 - Reduced Inequalities SDG 16 - Peace, Justice and Strong Institutions
01 Ethical Frameworks in Genetic Research +
This session will explore various ethical frameworks that guide genetic research, focusing on the principles of autonomy, beneficence, and justice. Participants will discuss the implications of these frameworks on research design and implementation.
02 Informed Consent in Genetic Testing +
This track will examine the complexities of obtaining informed consent in genetic testing, particularly in relation to the understanding of risks and benefits. Discussions will include strategies to enhance patient comprehension and autonomy.
03 Privacy and Data Protection in Genetic Research +
This session will address the ethical challenges surrounding privacy and data protection in genetic research. Experts will analyze current regulations and propose best practices for safeguarding sensitive genetic information.
04 Ethical Challenges in Gene Editing +
This track will focus on the ethical dilemmas posed by advancements in gene editing technologies, such as CRISPR. Participants will engage in discussions about the potential societal impacts and moral considerations of gene modification.
05 Personalized Medicine: Ethical Considerations +
This session will investigate the ethical implications of personalized medicine, particularly in relation to equity and access. Discussions will center on how personalized approaches can both benefit and challenge existing healthcare systems.
06 Confidentiality in Genetic Counseling +
This track will explore the ethical obligations surrounding confidentiality in genetic counseling. Participants will discuss the balance between patient privacy and the need for information sharing in clinical practice.
07 Research Integrity in Genetic Studies +
This session will focus on the importance of research integrity in genetic studies, emphasizing ethical conduct and accountability. Participants will examine case studies highlighting breaches of integrity and their consequences.
08 Patient Rights in Genetic Research +
This track will delve into the rights of patients involved in genetic research, including the right to withdraw and the right to be informed. Discussions will address how to uphold these rights while advancing scientific knowledge.
09 Ethical Governance in Genetic Research +
This session will explore the role of ethical governance in overseeing genetic research initiatives. Participants will discuss frameworks for ethical review and the importance of stakeholder engagement.
10 Ethical Use of Genetic Information +
This track will examine the ethical considerations surrounding the use of genetic information in both clinical and research settings. Discussions will focus on the potential for misuse and the need for ethical guidelines.
11 Emerging Ethical Issues in Genetic Technologies +
This session will address emerging ethical issues related to new genetic technologies and their applications. Participants will engage in forward-looking discussions about the implications for society and healthcare.