SiTec PharmaBio offers to pharmaceutical and biotechnology companies services in key areas of R&D, from lead and drug candidate selection to early clinical development.
- Formulation Development
- Analytical Development and Validation
- Regulatory Compliance
- Products development for Hospital use
- Strategic and technical support to start-up companies
- Professional Training as authorised agent for CfPA
We can support and manage experimental programs working directly with the Client at its own facilities.
At SiTec we established a network of Qualified Experts in specific areas of pharmaceutical development, such as regulatory, QA/QC, bioinformatics, in vitro models (cells and tissues) for biological characterization of drugs and formulations.
This feature allows us to support, conduct and manage experimental programs outside the client's facilities.