Fully Integrated Biologics CDMO site in Vilnius

Located in the vibrant heart of Lithuania’s high-tech sector, our Vilnius site is a cornerstone of European biopharmaceutical production. The facility leverages a deep local talent pool and cutting-edge infrastructure to deliver reliable, end-to-end solutions for global healthcare partners.

Location

Lithuania: A Rising Power in Global Biotech

Lithuania has emerged as a global leader in biotechnology, with a sector that has grown over 170% in recent years and a national commitment to reach 5% of the country’s GDP by 2030. This thriving ecosystem provides the ideal, high-innovation landscape to accelerate your molecule from concept to commercial reality.

170%+

Lithuanian biotech sector growth in recent years

5%

Target share of national GDP by 2030

12,000 m²

Biologics facility size in Vilnius

2

Interchangeable EU & US sites
The Facility

World-Class Facilities for Clinical and Commercial Supply

Our facilities in Vilnius, dedicated to protein-based biologics, provide a seamless, vertically integrated pathway from cell line development through cGMP manufacturing of drug substance and drug product. We offer the rare flexibility of both microbial and mammalian expression platforms, featuring six independent mammalian production lines and three microbial lines designed for stable manufacturing. Every project is underpinned by rigorous quality systems, supported by meticulous documentation to accelerate your molecule’s journey to the clinic.

40+

Number of R&D laboratories

12,000

Biologics facility size (m²)

FROM 10 L TO 4,000 L

Mammalian bioreactors (single-use)

FROM 10 L TO 4,500 L

Microbial fermenters

cGMP MANUFACTURING

Drug Substance and Drug Product

ASEPTIC FILL & FINISH

Vials, Pre-Filled Syringes, Lyophilization

Our
services

Cell Line & Strain Development

Developing high-producing mammalian cell lines and optimized microbial expression systems.

Process Development (USP & DSP)

Developing and optimizing robust bioprocesses for scalable manufacturing.

Analytical Development

Development, qualification and validation of phase-appropriate analytical methods.

cGMP MANUFACTURING

cGMP drug substance / product manufacturing for clinical and commercial supply with scalable production capabilities.

Viral Clearance Studies

Early and late-phase VCS for validation of purification processes to ensure robust downstream performance.

Quality & Regulatory CMC Support

Integrated QA, QC, and CMC regulatory excellence from development through commercialization.

ONE PARTNER. TWO CONTINENTS. ZERO COMPROMISE.

Our EU and US sites operate as one, same capabilities, same standards, full regulatory flexibility.

2025 CDMO Leadership Awards — Global BiologicsOutsourced Pharma & Life Science Connect
2025 CDMO Leadership Awards Europe — BiologicsOutsourced Pharma & Life Science Connect