ICCTRELC · Registering as Listener

International Conference on Clinical Trials, Research Ethics, and Legal Compliance

📅 5–6 May 2027 📍 Rijeka, Croatia 👤 Standard / Listener

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$165

virtual · $165 in person

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Supporting global researchConnect with researchers across 30+ countries

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Conference session tracks

Key research areas covered across the sessions — tap a track to read more.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.