Polpharma Biologics is a division of Polpharma Group, an established pharmaceutical company that is regularly inspected by the FDA and European competent authorities.
At Polpharma Biologics, we designed our facility and processes to be in full compliance with the requirements of all highly regulated markets. Our staff is thoroughly trained in cGMP and relevant ICH quality guidelines and adhere to these principles across all functions and activities.
Analytical Methods: In-Process Control and Product Release Testing
- Drug substance and drug product in-process control
- Drug substance and drug product release testing
Facility & Environment Control
- Environmental monitoring of cleanrooms
- Monitoring of utilities (water, steam and gas systems)
- Stability studies
- Leachables and extractables