Stason Pharmaceuticals

Established in 1994, with 25 employees, we’ve been manufacturing pharmaceutical products for our clients in the US and overseas. We are specialized in highly potent tablets and capsules such as anti-cancer medicines and immunosuppressants.

Products and Services

cGMP, registered with FDA, Japan’s PMDA and Health Canada
30 Year Experience in filing ANDAs, INDs/NDAs
High Potency suites: OEL 0.5 µg/m3 or less
Clinical trial materials and placebo manufacturing with depot services
Testing: Active Assay per USP, Bulk and Finished Product Release, Raw material per monographs, Impurity Analysis
DEA Analytical Permit
Stability: Long Term Stability, Accelerated Conditions, Finished Product Stability, Stability Storage
Residual Solvents
Warehouse is licensed to store and distribute drug products and medical devices

Manufacturing Processes

• Tablet compression and encapsulation, including modified release dosage forms
• Our production scales can go from sub-kilogram to 600 kg per lot
• Packaging