WHO’s principles for human genome data collection, access, use, and sharing: shaping ethical and inclusive genomics

11 February 2025 13:00 – 15:00 CET
Virtual Zoom webinar

The publication of the "WHO Guidance for human genome data collection, access, use and sharing" in November 2024 marks a major milestone in advancing ethical standards for genomic data globally. For the first time, a comprehensive set of principles has been established to ensure respect for individual rights, promote equity, and foster collaboration.

This webinar provides a unique opportunity to hear directly from WHO experts and global leaders about the guidance and its practical implications for research, policy, and healthcare systems.

Key Areas of Focus:

  • Promoting equitable access to genomic technologies and data.
  • Embedding ethical considerations into research and public health.
  • Simplifying data-sharing while ensuring privacy.
  • Strengthening the role of genomics in health systems.
  • Building global collaboration for ethical genomic research.

Target Audience:

This event is designed for a wide range of stakeholders, including:

  • Policymakers: Government agencies, regulatory bodies, and international organizations responsible for health policies and genomic data governance, including WHO.
  • Healthcare and Research Institutions: Leaders and administrators involved in integrating genomics into healthcare systems and research frameworks.
  • Researchers: Academics and industry professionals engaged in genomic data collection, sharing, and analysis.
  • Ethicists: Experts dedicated to addressing ethical challenges in genomic data governance and its applications.
  • Advocacy Groups and Civil Society: Organizations and advocates promoting equity and ethical practices in health and genomics.
  • Funders: Public and private organizations supporting genomics research and initiatives.

This broad audience ensures an inclusive dialogue, fostering collaboration to address challenges and opportunities in genomic data governance globally.

Objectives:

  • Understand WHO’s principles for advancing ethical genomic data sharing.
  • Explore how stakeholders can align practices with the guidance.
  • Discuss integrating genomics into health systems.
  • Share strategies for addressing challenges in data sharing.

Don’t miss this chance to engage with WHO and global experts on shaping the future of ethical genomic data sharing!