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