Capability
cGMP Finished Dosage Manufacturing
Integrated production of tablets, capsules, blends, and ready-to-fill intermediates. Cross-functional teams manage process validation, packaging readiness, and release testing.
Tablets
Direct compression & coated formats
Capsules
Blends and microencapsulated actives
Premixes
Ready-to-fill intermediates for partners
Packaging
Blister, bottle, and bulk configurations
Capabilities & Benefits
- Process readiness: Equipment selection and settings defined during development
- In-process controls: Weight, hardness, friability, and dissolution monitoring
- Quality system: cGMP, ISO 9001:2015, and data integrity controls
- Regulatory support: Batch documentation, validation, and stability programs
Commercialization Support
- Tech transfer: Structured protocols and training for partner sites
- Supply continuity: Redundant sourcing and traceable warehousing
- Packaging readiness: Compatibility assessments and shelf-life studies
- Project management: Dedicated leads coordinating timelines and deliverables