Facility
-Approximately 20k sqft of laboratory, processing suites, warehouse, and office space.
-Quality and operating systems designed for pre-registration development and clinical manufacturing activities.
-Includes seven state-of-the-art processing suites designed to meet quality and safety standards of both pharmaceutical clients and regulatory agencies.
-Temperature controlled warehouse
-Separate laboratories for R&D/pre-formulation and in-process testing/QC
Development and Pilot Scale Processing Equipment
-Blending and milling
-Particle engineering by spray drying and micronization
-Dry and wet granulation
-Tablet compression and coating
-Gravimetric encapsulation
Analytical and Laboratory Instrumentation
-Thermal analysis including (mDSC, TGA, DVS)
-API form analysis (XRD)
-Chemical analysis (HPLC, UPLC, UV-vis, KF)
-Bio-relevant dissolution testing and colloidal characterization
-Dosage form and granule mechanical characterization (Envelope and true density, compaction analysis)
-Light and electron microscopy
-Stability chambers for ICH zones
-Particle characterization for oral and inhaled drug products (particle size, NGI, DDU)
Facility
-Approximately 20k sqft of laboratory, processing suites, warehouse, and office space.
-Quality and operating systems designed for pre-registration development and clinical manufacturing activities.
-Includes seven state-of-the-art processing suites designed to meet quality and safety standards of both pharmaceutical clients and regulatory agencies.
-Temperature controlled warehouse
-Separate laboratories for R&D/pre-formulation and in-process testing/QC
Development and Pilot Scale Processing Equipment
-Blending and milling
-Particle engineering by spray drying and micronization
-Dry and wet granulation
-Tablet compression and coating
-Gravimetric encapsulation
Analytical and Laboratory Instrumentation
-Thermal analysis including (mDSC, TGA, DVS)
-API form analysis (XRD)
-Chemical analysis (HPLC, UPLC, UV-vis, KF)
-Bio-relevant dissolution testing and colloidal characterization
-Dosage form and granule mechanical characterization (Envelope and true density, compaction analysis)
-Light and electron microscopy
-Stability chambers for ICH zones
-Particle characterization for oral and inhaled drug products (particle size, NGI, DDU)
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