Genuine quality by design

Our purpose-built Belgian facility represents our committed investment in pharmaceutical supply, designed specifically to comply with the highest-level of EU requirements.

Every operational area is optimized for regulatory compliance, process efficiency, and product integrity, from GMP-certified production environments to validated multi-temperature GDP storage systems.

Built with the future in mind

Advanced monitoring, backup systems, and adaptable production configurations combined with room for new building developments, enable Novitan's response to evolving clinical trial requirements across global markets.

With validated computer systems, continuous environmental controls, and strategic European positioning, Novitan is ideally positioned to support pharmaceutical development programs with the operational reliability and regulatory compliance that international studies require for successful execution.
4459
Sqm total facility space
24/7
Environmental monitoring
100%
Reusable / green energy

Located in the heart of Europe

Belgium's regulatory framework enables direct importation of investigational medicinal products without additional licensing requirements, streamlining international supply chain operations for pharmaceutical companies conducting global clinical trials.

Combined with established European Union market access and comprehensive regulatory knowledge, Novitan provides efficient coordination capabilities for complex international studies.