Expanding the Horizon of Advanced Therapies: Our Gene Therapy Center

Located within Baltics’ leading biotechnology hub, our new Vilnius site provides the specialized infrastructure and expertise required for complex genetic medicine development.

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

8,000 m²

Dedicated gene therapy facility size

20+

R&D laboratories on site
The Facility

Dedicated Manufacture of Gene Therapy Products

Our state-of-the-art 8,000 m² facility in Vilnius provides a fully integrated CDMO platform for the rapid development and cGMP manufacture of viral vectors and plasmid DNA. This purpose-built center features specialized biosafety suites designed for seamless scale-up from process development to commercial supply. Our capabilities encompass the full production lifecycle, including high-purity pDNA starting materials, upstream viral vector production, and sophisticated downstream purification. We ensure maximum process efficiency and rigorous regulatory compliance for next-generation genetic medicines.

20+

Number of R&D laboratories

8,000

Gene Therapy facility size (m²)

FROM 45 L - 450 L

pDNA fermentation range

FROM 10 L - 1,000 L

Viral vector bioreactor range

FROM 50 L - 200 L

BSL-3 manufacturing suites

ASEPTIC FILL & FINISH

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.