QbD Group

QbD Group is a Belgian life sciences consulting firm supporting pharma, biotech and medtech companies from idea to patient. With 600+ experts across regulatory affairs, quality assurance, clinical services and GMP compliance, we help organisations navigate complex regulatory frameworks, including the stringent requirements that apply to radiopharmaceuticals and short-lived isotope-based products.

Belgium is one of Europe's most active hubs for nuclear medicine, and the regulatory and quality demands in this space are uniquely challenging: accelerated production timelines, hospital exemptions under EMA guidelines, specific GMP annexes, and evolving clinical evidence requirements. QbD brings deep EU regulatory expertise and a hands-on, pragmatic approach that fits the pace and complexity of this environment.

Whether you're developing a new radiopharmaceutical, managing GMP compliance at a cyclotron facility, or preparing a clinical dossier for a PET tracer, we work as an extension of your team to get it done right.