
Active Pharmaceutical Ingredients
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3 ISO Class 8 API Suites
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Lead Candidate Synthesis
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Reference Standards Synthesis
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cGMP API Synthesis and Purification (mg - Multi Kg Batch Sizes)
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Designated Manufacturing and Storage Areas
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DEA Licensed (Schedule II)
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Lab Scale Hydrogenation (High Pressure and Low Pressure) Capabilities
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In-house Stability and QC Testing