Bioethics & Governance
Genome editing, AI in biology and dual-use research raise ethical and governance questions that move faster than regulation. The session covers CRISPR germline editing guidelines after the He Jiankui case and the WHO 2024 framework, AI ethics in medical decision-making, biosecurity frameworks for synthetic biology, informed consent for advanced therapies including pediatric gene therapy, dual-use research of concern (DURC), and global regulatory harmonisation efforts. Discussion addresses public engagement in biotechnology decisions, indigenous data sovereignty in genomics, the ethics of human-animal chimeras, AI explainability requirements for medical decisions, and the patenting of CRISPR-related inventions.
- CRISPR germline editing guidelines
- AI ethics in medical decisions
- Biosecurity frameworks
- Informed consent for gene therapy
- DURC framework
- Indigenous data sovereignty
- Chimera ethics
- CRISPR patent landscape
Explore the full GSBG 2027 program
- 01Synthetic Biology & Biomanufacturing
- 02Genetic Engineering & CRISPR
- 03Tissue Engineering & Biomaterials
- 04Medical Devices & Sensors
- 05Bioinformatics & Computational Biology
- 06Drug Delivery Systems
- 07Biomechanics & Prosthetics
- 08Regulatory & Bioethics
- 09Industrial Biotechnology
- 10AI in Drug Discovery
- 11Cell & Gene Therapy
- 12Stem Cell Research
- 13Antibody-Drug Conjugates
- 14Vaccines & Immunotherapy
- 15Microbiome Engineering
- 16Nanomedicine
- 17Personalized Medicine
- 19Marine Biotechnology
- 20Plant Biotechnology
- 21Agricultural Biotech
- 22Environmental Biotech
- 23Single-Cell Biology
- 24Spatial Biology
- 25Organoids & Organ-on-Chip
- 26Lab Automation
- 27Biosecurity
- 28Synthetic Genomics
- 29Bioprinting
- 30Biosensors & Diagnostics
- 31Liquid Biopsy
- 32Multi-Cancer Early Detection
- 33Continuous Biomanufacturing
- 34Decentralised Manufacturing
- 35RNA Editing