Your biotech projects deserves more than a supplier. It needs a partner.
Let’s meet at CPHI Frankfurt
Booth 6.1D50
Book a meeting with our team at CPHI Frankfurt.
Scientific expertise, GMP compliance and operational flexibility—your biotech CDMO partner at every step.
Integration and continuity
End-to-end workflow from development to manufacturing and QC.
Tailor-made approach
Custom solutions built around each project’s unique challenges.
Proactive collaboration
Fast, open communication and a partner mindset at every step.
Mammalian & Microbial R&D
Custom development of biologics using bacterial and mammalian cell systems—designed for smooth scale-up and tech transfer.
GMP Clinical Manufacturing
Production of clinical-grade biologics (APIs) via microbial fermentation, with full GMP compliance and batch documentation.
Sterile Fill & Finish
Aseptic filling of liquid drug products for clinical trials, in compliance with GMP and Annex 1 requirements.
Who we support
Biotech & Pharma Companies
End-to-end CDMO support for the development, production, and release of biologics.
Biotech Startups
Agile, expert-backed solutions to bring your molecule from lab to clinic.
Research Institutes & Universities
Tech transfer services to turn academic research into real-world therapeutics.
Q&A
- Are your CDMO services scalable?
-
Yes. We adapt to evolving project needs while maintaining quality and regulatory standards.
- Can I request a fully customized biotech solution?
-
Absolutely. Our scientific team works closely with clients to co-design solutions that fit each specific challenge.
- Who will I meet at the Diatheva stand during CPHI?
-
You’ll meet experts from our R&D, GMP manufacturing, and business development teams—ready to discuss your project in depth.
