Nuclear Medicine in Belgium

14 – 15 Oct 2026 | Suarlée, Belgium

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Thursday, 15 October 2026 | 11:00 - 12:00

Thematic Session 2 – Regulatory excellence as a driver of innovation: Aligning ecosystem actors (industry, clinics & authorities)

Location:Salle ImpressionnisteTrack:Regulatory Pathways & Access
  • Nuclear medicine
  • Radioligand therapy (RLT)
  • Health innovation
  • Diagnostics
  • Clinical innovation
  • Patient impact
  • Clinical trials
  • Innovation ecosystem
  • Public-private partnerships
  • Collaboration
  • European collaboration
  • International collaboration
  • Academic-industry collaboration
  • Europe
  • Regulatory excellence
  • Regulatory pathways
  • Market access

This session will bring together industry leaders, clinicians, academics, and Belgian regulatory authorities (FANC & FAMHP) to explore how regulation can better align with innovation and patient needs.

Key discussion points include:

  • How regulatory frameworks influence the development of cutting-edge therapies

  • The journey from “first-in-class” innovation to patient access

  • The real impact of regulatory pathways across the entire value chain

  • Challenges and expectations from both innovators and regulators

  • Insights from international practices beyond Belgium and Europe

The session will also feature:

  • A practical case study on deploying a clinical trial network in radioligand therapy

  • Real-world examples of how collaboration can accelerate access while ensuring compliance

Why attend?

Discover how different stakeholders can work together to create a more agile, innovation-friendly regulatory environment, and identify actionable solutions to bring therapies to patients faster.

1 speaker

  • MD PhD nuclear medicine specialist

    Vrije Universiteit Brussel