NovaPharma B.V. is a leading contract development and manufacturing organization headquartered in Netherlands. We specialize in Commercial Manufacturing, Small Molecule API Manufacturer with state-of-the-art facilities serving clients globally.
Biologics Drug Product, Lyophilization, Regulatory Support, Small Molecule Drug Product, Viral Vectors
1 site worldwide
Our flagship service offering for Infectious Disease and Ophthalmology applications.
Our specialized service offering for Rare Disease applications.
Our flagship service offering for Cardiovascular applications.
3 published case studies showcasing past projects, challenges and outcomes.
Successful Phase I manufacturing program for a virtual pharma client.
The client required rapid scale-up of their CNS (Central Nervous System) therapeutic with aggressive timelines and complex analytical requirements.
We deployed our experienced team and state-of-the-art facilities to develop a robust manufacturing process. Key innovations included process intensification and real-time analytics.
The program achieved all milestones on schedule. The product received regulatory approval and is now in commercial production.
Successful Discovery manufacturing program for a emerging biotech client.
The client required rapid scale-up of their Dermatology therapeutic with aggressive timelines and complex analytical requirements.
We deployed our experienced team and state-of-the-art facilities to develop a robust manufacturing process. Key innovations included process intensification and real-time analytics.
The program achieved all milestones on schedule. The product received regulatory approval and is now in commercial production.

A comprehensive overview of how NovaPharma B.V. successfully delivered this complex pharmaceutical manufacturing project.
The client required rapid scale-up while maintaining strict quality standards and regulatory compliance. Time-to-market was critical.
Our team implemented innovative process optimization techniques, leveraged advanced manufacturing technologies, and established robust quality control systems.
Project completed 30% faster than industry average with zero quality deviations. Client achieved regulatory approval on first submission.


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