The Role of Newborn Genetic Screening in Healthcare in Luxembourg

Understanding, discussing, and shaping the future together!

On 20 and 21 November 2026, the Health Directorate is organising a national conference dedicated to the role of newborn genetic screening in healthcare in Luxembourg.

The event will bring together healthcare professionals, experts, patient representatives, and members of the public to discuss scientific advances, the opportunities and limitations of newborn genetic screening, as well as the ethical and societal issues it raises.

Registration is now open!

Two insightful days

• Friday, 20 November 2026 | 13:00 – 19:00
  Scientific Programme
  Presentations and discussions focusing on scientific advances, international experiences, healthcare pathways, data use, and the ethical and societal implications of newborn genetic screening.
• Saturday, 21 November 2026 | 09:00 – 17:00
  Public Conference
  A day open to everyone, featuring accessible presentations, personal experiences shared by families, a public debate, and interactive workshops.

Three thematic workshops will take place on Saturday from 14:00 to 15:00:

1. Workshop A: Under what conditions could a newborn genetic screening programme be considered?
2. Workshop B: What safeguards are needed to protect genetic data?
3. Workshop C: How can families best be informed and supported?

Participation in the workshops requires advance registration, which can be completed directly through the registration form.

• View the detailed programme (Pdf - 213 Kb)

Free admission – Registration required

Simultaneous interpretation in French and English will be available upon request. Language requirements can be specified in the registration form.

Participants may register for either one or both days, and for one of the three workshops offered on Saturday.

Register for the conference