Active Pharmaceutical Ingredients

• 3 ISO Class 8 API Suites

• Lead Candidate Synthesis

• Reference Standards Synthesis

• cGMP API Synthesis and Purification (mg - Multi Kg Batch Sizes)

• Designated Manufacturing and Storage Areas

• DEA Licensed (Schedule II)

• Lab Scale Hydrogenation (High Pressure and Low Pressure) Capabilities

• In-house Stability and QC Testing