From DNA to Product: Code Better Through Tuning…
summary
An expert in quality/QA/regulatory affairs and a data product manager describe building a genomics AI health product under strict regulations (GDPR, CE marking, EU AI Act). They explain concrete engineering and product practices the project used—auditability, human supervision, versioning, documentation—to ensure reliability, explainability and compliance. The talk argues regulatory constraints can drive better technical practices and greater product impact.
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chapters (11)
- 0:00Introduction
- 1:10Endometriosis case study
- 2:12Medical data collection challenges
- 3:57Medical coding best practices
- 6:44AI explainability in medicine
- 8:49Medical reproducibility and testing
- 10:13Data security in healthcare
- 12:58GDPR and health ethics
- 14:01Medical algorithm biases
- 15:25MDR and AI Act regulations
- 15:45Conclusion
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