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