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- Active ingredients
- Generics in bulk
and/or packed
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Calao has a portfolio of APIs complying with EU and FDA requirements, of which some are of Italian origin and others are selected from foreign sources with a specific expertise.
The reliability of the sources is monitored by audits carried out periodically at the supplier’s site.
The relationship between Calao and the supplier is grounded on long term technical and cooperation agreements.
European Drug Master File is available for most of the APIs.
For products enlisted in Ph. Eur. our first target is the obtainment of the Certificate of Suitability (CoS).
Starting from some of its APIs Calao has successfully developed generic formulations. |
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