Transfer Of Commercial Scale Processes
Source: Uquifa S.A.U.

All UQUIFA's sites operate under cGMP conditions and have been inspected and approved by the FDA, EDQM, ANVISA and/or KFDA.
In addition to the regular production programs, Uquifa offers the opportunity to manage the development activities of any drug life cycle by offering services on DMF/CTD/COS application, stability studies, process validation and analytical method validation, working standard supply or impurity characterization.
- Process transfer
- Process development and improvement
- Analytical methods development
- Scale up to commercial
- Reference standards synthesis
- Impurity profile characterisation
- Stability Studies
- Polymorphism Studies
- Regulatory support and file submission and maintenance
Need More Information? Just Ask.
Click the button below to directly contact the supplier. Use it to:
- Ask a question.
- Request more detailed information or literature.
- Discuss your current project/application.
- Request a quote.
- Locate a distributor in your area.
- Schedule a demo.
Uquifa S.A.U.
This website uses cookies to ensure you get the best experience on our website. Learn more