Our manufacturing plants are fully GMP and WHO certified, ensuring every batch meets international safety and efficacy standards.

Yes, we provide end-to-end CDMO services including formulation development, clinical trial supply, and large-scale commercial production.

Standard production cycles typically range from 4 to 6 weeks, depending on raw material availability and specific testing requirements.

We utilize a fully digitized Electronic Batch Record (EBR) system to ensure 100% traceability and data integrity throughout the lifecycle.

Absolutely. We provide comprehensive stability data and CMC documentation to support your submissions to the FDA, EMA, or local authorities.

We combine cutting-edge automation with a rigorous QA culture, delivering high-potency and specialized medicine with zero-defect goals.