LEADING END-TO-END CDMO FOR PROTEIN-BASED BIOLOGICS AND ATMPs​

Science-driven. Flexible. Built around your program.

Offerings

From monoclonal antibodies to complex recombinant proteins, our integrated mammalian capabilities support biologic programs from early development through clinical manufacturing and toward commercialization.
From recombinant proteins to complex microbial-derived biologics, our integrated bacterial and yeast capabilities support programs from early development through clinical and commercial manufacturing.
From plasmid development to scalable GMP manufacturing, our integrated pDNA capabilities support advanced therapy and biopharmaceutical programs through development, scale-up, and clinical manufacturing.
From vector and process development to cGMP manufacturing, our integrated viral vector capabilities support gene therapy programs from early development through clinical manufacturing.
From process development to cGMP manufacturing, our integrated cell therapy capabilities support complex living-cell products through advanced processing, analytics, and purpose-built manufacturing infrastructure.

ADCs

ADCs service coming in Q2 2027

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.

220+

Successful projects globally.

22

Years of CDMO
experience

110+

Satisfied clients worldwide

200+

Bioprocessing experts

4

EMA & FDA
compliant sites

Don't take our word for it

Hear it from our clients.

Innovative and Fast-Growing CDMO

We operate four state-of-the-art facilities designed to support your program at every stage. Our European and US-based sites work seamlessly together, delivering integrated solutions from cell line development to cGMP manufacturing at scale. Wherever you are, we are within reach. 

End-to-end mammalian and microbial biologics development and cGMP manufacturing, from cell line and process development to drug substance and aseptic drug product.
End-to-end mammalian and microbial biologics development and cGMP manufacturing, integrating drug substance and drug product capabilities.
End-to-end plasmid DNA and viral vector development and cGMP manufacturing, with dedicated BSL-2 viral clearance and BSL-3 laboratory capabilities.
End-to-end development and cGMP manufacturing of autologous and allogeneic cell therapies, with integrated 3D bioprinting capabilities.

22/09/2026

BPI Conference & Exhibition

06/10/2026

CPhI / BioProduction

13/10/2026

Festival of Biologics

27/10/2026

ESGCT

09/11/2026

Bio-Europe

Contact us

Please tell us about your project and the challenges you are facing. The more detail you share, the better we can tailor our response. A member of our team will follow up shortly to discuss how Northway Biotech can support your biopharmaceutical product’s success.