- Formulation development
- Dosage form development
- Analytical chemistry
- Methods development and validation
- Stability programs
- In vitro BA/BE testing
- Process development
- State-of-the-art cGMP/GLP facility
- Class 100,000 filling suites for pMDIs, DPIs, nasal and buccal sprays
- Process development and scale up
- Pilot scale manufacturing
- Preclinical, toxicology and clinical supplies
- Dedicated space, staff and equipment available
- Process validation
- Supply chain management
- Labeling and packaging services
- Warehousing
