Research
In-house R&D teams advance therapies from molecule to medicine.
Belgian Pharmaceutical LaboratoryPrecision pharmaceuticals.
Precision pharmaceuticals.
Belgian craftsmanship.
At Veltrane Laboratories we research, formulate and manufacture medicines you can trust — built on European standards of quality, safety, and care.
Certified
EU-GMP · ISO 9001 · FAGG
- 1998
- Founded
- 120+
- Products
- 27
- EU markets
Veltrane is registered with the Belgian Federal Agency for Medicines and Health Products (FAGG / AFMPS).
Our mission
Three pillars guide every formulation
From early research through final release, our work is anchored in scientific rigor and uncompromising quality.
Quality
Every batch passes multi-stage analytical and microbiological control.
Trust
Transparent sourcing, traceable manufacturing, patient-first values.
Therapeutic areas
A focused product portfolio
Cardiovascular
ACE inhibitors, statins, beta-blockers and more for heart health.
BrowseAntibiotics
Broad- and narrow-spectrum agents for infectious disease management.
BrowseRespiratory
Inhaled therapies for asthma, COPD and chronic respiratory care.
BrowseVitamins & Supplements
Pharmaceutical-grade vitamins, minerals and omega formulations.
BrowseWhy Veltrane
European standards. Belgian precision.
Our Brussels facility operates under EU-GMP guidelines with a fully integrated quality management system. Every step of production — from raw material qualification to final batch release — is documented, validated, and independently audited.
- EU-GMP certified manufacturing
- In-house analytical and microbiological labs
- Serialization and traceability on every batch
- Continuous pharmacovigilance program
EU-GMP
European Good Manufacturing Practice
ISO 9001:2015
Quality management systems
FAGG / AFMPS
Belgian Federal Agency for Medicines and Health Products
ISO 17025
Laboratory accreditation
Quality control
Five steps from raw material to release
- Step 1
Raw material qualification
Identity, purity and potency testing of every incoming material.
- Step 2
In-process control
Inline checks during formulation, granulation and packaging.
- Step 3
Analytical testing
HPLC, dissolution, content uniformity and microbiological assays.
- Step 4
Stability program
Long-term and accelerated studies in ICH-compliant chambers.
- Step 5
Qualified person release
Final batch certification by a designated EU Qualified Person.
Questions about a product or batch?
Our medical and quality teams respond to every inquiry within two business days.