Brochure
17 Sep 2021

Contract Development and GMP Manufacturing Services

PDF 11.4 MB

We are well positioned to efficiently and expertly support your entire project at all stages of biopharmaceutical development, from cell line generation through process development. 

In our state-of-the art GMP production facility authorized by EMA we produce and release biological Active Pharmaceutical Ingredients (APIs) for preclinical and Phase I/II clinical trials.

Content provided by our supplier

DIATHEVA

  • IT
  • 2019
    On CPHI since
  • 3
    Certificates
  • 1 - 24
    Employees
Company types
Biopharmaceutical company
CMO/CDMO
Contract Service
Manufacturer/Innovator
Primary activities
API Producer
Biopharmaceutical
Contract Manufacturer

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