Flyer: Sterile manufacturing – finished dosage forms
Posted: 23 January 2019 | Eurofins CDMO | No comments yet
Eurofins CDMO provides a wide range of aseptic processing services for all drug product configurations with flexibility to accommodate a wide range of compounds, primary packaging systems, batch sizes and fill volumes to help develop your Active Pharmaceutical Ingredient or bulk product into Finished Dosage Forms for use in clinical trials and commercial purposes.
- Sterile fill & finish activities for chemical and biological entities under full global, GMP-compliance.
- Authorisations for nearly all drug substances and ability to handle biotech products, nanocarriers, highly potent products and controlled substances.
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Active Pharmaceutical Ingredient (API), Clinical Trials, Ingredients, Manufacturing, Packaging, Regulation & Legislation
