Clinical Trials, Biotech Regulations & Global Compliance

This track provides a comprehensive overview of regulatory science in the era of biotechnology. Experts will explore innovations in clinical trial design including decentralized, adaptive, and real-world evidence based models. Sessions will address multi-regional approvals, CTA submissions, GMP/GLP compliance, and post-marketing surveillance. Thought leaders will share strategies to enhance trial diversity, patient engagement, and regulatory navigation. Participants will leave equipped with practical tools for ensuring quality, ethics, and global regulatory alignment.

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