Production Division

The plant of Sicor Biotech UAB consists of:

• Certified 800 m2 clean production facilities with modern infrastructure.
• Water and purified steam production equipment.
• Bioreactors with CIP/SIP systems.
• Centrifuges for cells and protein recovery.
• Chromatographic purification systems for protein purification.
• In-process control lab.
• Raw material warehouses and product quality control labs.

The plant currently produces two active pharmaceutical ingredients (API): recombinant human granulocyte colony stimulating factor (Filgrastim) and recombinant human interferon alfa-2b. These APIs form the basis for Tevagrastim, a biological medical product registered in all the EU, Grasalva and Realdiron drug products..
The quality of our products complies with the requirements of the European Union (EU), the United States of America (USA), and the World Health Organisation (WHO). The quality of all APIs is strictly monitored in conformity with the requirements. The entire production process is compliant with the current Good Manufacturing Practice (cGMP) requirements. The company has received the appropriate national and international certificates of conformance to cGMP.