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Join the International Symposium on Medical Ethics and Clinical Trials (ISMECT-26), a hybrid event in Dubai, UAE, designed for researchers and professionals to share the latest insights and network with global experts in the field.
The International Symposium on Medical Ethics and Clinical Trials (ISMECT-26), organized by the Atlantic Federation for Technical Education & Research (AFTER), is a premier international event for academics and industry professionals. This hybrid conference provides a dynamic platform to showcase the latest advancements and innovations in the field, exchange ideas, and discuss new developments. Attendees can participate either in person in Dubai or online, taking full advantage of opportunities to disseminate research, network with a global community of experts, and accelerate their careers through engaging presentations, expert panels, and keynote speeches from global thought leaders.
A review of the fundamental principles of autonomy, beneficence, non-maleficence, and justice as they apply to clinical trials.
Best practices and challenges in obtaining meaningful and voluntary informed consent from research participants.
Strategies for protecting participant data and ensuring confidentiality throughout the research lifecycle.
Guidelines for designing clinical trials that are scientifically sound and ethically robust.
Navigating the complex landscape of national and international regulations governing clinical research.
Understanding the function and importance of IRBs and ethics committees in safeguarding research participants.
Ethical considerations when including children, pregnant women, prisoners, and cognitively impaired individuals in clinical trials.
Addressing ethical issues in international research collaborations, particularly in low-resource settings.
The importance of involving communities in the research process to ensure cultural sensitivity and relevance.
Exploring the ethical implications of using artificial intelligence and large datasets in clinical studies.
Identifying and managing financial and non-financial conflicts of interest in clinical research.
Discussing the responsibilities of researchers and sponsors to participants and communities after a trial concludes.
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