Custom Biotech Solutions for Your Projects.
End-to-End Biotech CDMO Expertise Tailored to Your Needs.
With 20+ years of experience and a 70% Ph.D. team, Diatheva provides reliable, GMP Biotech CDMO solutions tailored to your needs.
Specialisation and reliability
We are a partner with extensive experience in the biotechnology sector, particularly in the production of APIs and biopharmaceutical finished products for every stage from preclinical to clinical trials.
Customization and adaptability
The ability to provide customized solutions tailored to the specific needs of our clients
Timeliness and responsiveness
Our quick response to emerging needs and our ability to meet deadlines are other distinctive aspects of our approach.
Mammalian & microbial r&d development and production
Comprehensive R&D services for the development and production of biologics through bacterial and mammalian cell lines.
Gmp manufacturing of clinical-grade biologics (apis)
GMP-compliant manufacturing services for clinical-grade biologics produced through bacterial fermentation.
Sterile fill & finish
Aseptic fill and finish services for liquid drug products intended for clinical trials in compliance with GMP and Annex 1 requirements
Who Can We Help ?
Biotech & Pharma Companies
Tailored CDMO solutions for R&D and manufacturing.
Biotech Startups
Accelerating biotech innovation with flexible and efficient solutions.
Research Institutes & Universities
Bridging the gap between research and commercialization.
Q&A
- What makes Diatheva different from other Biotech CDMO providers?
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We specialize in small-scale CDMO with a focus on flexibility, compliance, and tailored solutions.
- Are your CDMO services scalable?
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Yes, we adapt to client needs while maintaining GMP quality standards.
- Can I request a fully customized biotech solution?
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Absolutely. Our team works closely with clients to design tailored solutions that meet specific needs.
