BePharBel Manufacturing is your CDMO expert in formulation, reformulation and the manufacturing of sterile and non-sterile medicines for human and animal health.
Our mid-sized structure and integrated end-to-end solution ensure responsiveness, efficiency and quality at every stage—from R&D to market launch.
The result? Fast and optimized development of your medicines and medical devices.
End-to-End Services and EU-GMP Manufacturing
(Re)Formulation & Process Development
Analytical Methods (ICH)
Stability Studies
Technology Transfer & Production Scale-Up
EU-GMP Manufacturing
Packaging And QP Release
Regulatory Support & Supply Management
Choose our expertise, pragmatism, and commitment to building long-term partnerships.
Quality
Flexibility
Innovation
Transparency
Our Three Fundamental Pillars
1 Export Oriented
2 Partnership Approach
3 Long-term Commitment
Founded in 2012 by a group of experienced and active players in Belgian and international pharmaceutical development, our company is continuously strengthening its position in Belgium and Europe. Today, BePharBel Manufacturing works with more than 10 different dosage forms—solid, liquid, and semi-solid—and on over 40 finished products.
Our independence guarantees strong partnerships and long-term support to ensure your projects’ success.
MMCR
NEW PATENT
The revolutionary MMCR technology (Multi-layer Microparticle Controlled Release) enables the development of controlled release syrup (prolonged or delayed).
Our Certifications
- EU-GMP Manufacturing
- Manufacturing and Distribution Authorization for Human and Veterinary Medicines and Medical Devices
- Authorized IMP Manufacturer
- Manufacturing Authorization for Sterile Medicines, including injectables
How can we help you?