Regulatory and Ethical Challenges in Biomarker Development
As biomarker science advances rapidly, ethical and regulatory considerations have become crucial. This session examines global regulatory frameworks governing biomarker validation, clinical trial inclusion, and diagnostic approval. Experts will discuss data integrity, patient consent, and privacy concerns associated with biomarker research. The role of international harmonization in ensuring safety and compliance will be emphasized.
The track will also explore ethical dilemmas in biomarker-based genetic testing and data sharing. Attendees will gain insights into best practices for maintaining transparency and protecting patient rights while promoting innovation. By participating, delegates will understand how regulatory and ethical frameworks support sustainable, responsible biomarker development
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