The project will be carried out by our trusted and qualified CDMO partners and could be managed by PHC or clients. PHC is able to help you with partner sourcing for your critical projects. Once API early development is completed, our partners will synthesize and scale-up the APIs on an exclusive basis under full cGMP and in compliance with regulatory requirements and highest quality standards.
As an experienced and reliable contract development & manufacturing partner, we are supporting our customers from the preliminary idea to the submission of the final documentation.
Our API CDMO partner’s capabilities:
- General APIs
- High potency APIs and oncology APIs
- Sterile APIs
- β-lactam APIs
- Bulk lyophilization APIs
- Fermentation APIs
Our API CDMO Partners’ GMP Status and Locations:
- Taiwan, China &EU
- Compliance with US FDA, EU GMP, JP PMDA, KFDA and PIC/s GMP requirements