Hybrid Conferencee

International Conference on Clinical Trials, Research Ethics, and Legal Compliance (ICCTRELC - 26)

21st - 22nd October 2026 | Seoul, South Korea
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Conference Notifications:

"Be sure to check this section regularly for all Research Plus International Conference updates. We’ll keep you informed about deadlines, event details, and more important notifications."

Call for Papers Extended:
"The deadline for full paper submissions has been extended for the Research Plus International Conference in Seoul. Submit your research by today to participate in one of the top conferences."
Certificate of Presentation:
"Present your research and receive a Certificate of Presentation to recognise your valuable contribution to the conference."
Abstract Submissions Open:
"Abstract submissions for the Seoul event are now open! Don’t miss the chance to present your research. Submit now."
Networking with Global Experts:
"Engage with researchers and professionals from around the world at the Seoul conference. Build collaborations and gain insights from leading experts."
Keynote Speaker Sessions:
"Don’t miss our Keynote Sessions in Seoul, featuring global leaders and innovators sharing their knowledge."
Best Paper & Best Paper Presentation Award:
"Submit your paper and stand a chance to win the Best Paper Presentation Award. The winner will be recognized at the conference in Seoul."
SDG-Inspired Conference Focus:
"Our conference will highlight research that addresses global sustainability, inclusive education, and solutions for environmental challenges."

Conference Session Tracks

SDG Wheel

Aligned with

UN Sustainable Development Goals

This conference contributes to global sustainability by aligning its research discussions and academic sessions with key United Nations Sustainable Development Goals. It fosters knowledge exchange, innovation, and collaborative engagement.

SDG 3
SDG 3 Good Health and Well-being
SDG 16
SDG 16 Peace, Justice and Strong Institutions
Track 01

Ethical Considerations in Clinical Trials

This track will explore the ethical principles governing clinical trials, focusing on the balance between scientific advancement and patient welfare. Discussions will include informed consent processes and the role of ethics committees in trial oversight.

Track 02

Regulatory Frameworks in Health Care Law

This session will examine the various regulatory frameworks that govern clinical trials and health care practices. Participants will analyze the implications of these regulations on trial design, implementation, and patient safety.

Track 03

Good Clinical Practice and Compliance

This track will address the principles of Good Clinical Practice (GCP) and their significance in ensuring the integrity of clinical trials. Emphasis will be placed on compliance strategies that enhance trial governance and data reliability.

Track 04

Patient Safety and Risk Management

This session will focus on the critical aspects of patient safety within clinical trials, highlighting risk management strategies that protect participants. Discussions will include case studies illustrating effective safety protocols and incident response.

Track 05

Bioethics and Human Subjects Protection

This track will delve into the intersection of bioethics and legal compliance in the protection of human subjects in research. Topics will include ethical dilemmas and the role of institutional review boards in safeguarding participant rights.

Track 06

Data Integrity and Research Governance

This session will explore the importance of data integrity in clinical trials and the governance structures that support it. Participants will discuss best practices for ensuring accurate data collection and reporting.

Track 07

Legal Challenges in Clinical Research

This track will address the legal challenges faced by researchers in the context of clinical trials, including liability issues and compliance with health care laws. Experts will provide insights into navigating these complexities effectively.

Track 08

Informed Consent: Legal and Ethical Dimensions

This session will examine the legal and ethical dimensions of informed consent in clinical trials. Discussions will focus on the adequacy of consent processes and the implications of non-compliance.

Track 09

Trial Governance and Ethical Standards

This track will investigate the governance structures that uphold ethical standards in clinical trials. Participants will analyze the roles of various stakeholders in maintaining compliance and ethical integrity.

Track 10

Policy Compliance in Health Research

This session will focus on the importance of policy compliance in health research, examining the legal frameworks that guide researchers. Discussions will include strategies for ensuring adherence to both national and international regulations.

Track 11

Emerging Trends in Health Care Law

This track will explore emerging trends and challenges in health care law as they relate to clinical trials. Participants will discuss the impact of technological advancements and evolving regulations on research practices.