Professional OEM
Orient Pharma (OP) has passed FDA verification and PIC/S GMP certification, providing professional contract manufacturing and development services, including technology transfer, tablet production, capsule filling, and analysis services for clinical trial drugs or commercial batches.
Professional Formulation Technologies
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Semi-solid Multi-phasic Release Technology (SMRT) |
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Osmotic-controlled Release Oral Delivery System (OROS) |
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Multiple Unit Pellet Systems (MUPS) |
Main Formulation Technologies
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Three-stage liquid/semi-solid hard capsule filling |
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High-speed mixing granulation/bilayer tablet production |
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Laser-drilled tablet production |
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Glatt fluidized bed granulation/Wurster pellet coating equipment |
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Multi-stage pellet capsule filling |
Analytical Services
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Compliant with cGMP and capable of performing drug analysis according to USP/EP/BP/JP and non-pharmacographa standards |
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Equipped with USP dissolution analyzers I/II/III, HPLC, UPLC, GC, PSD, FTIR, UV, ICP-MS, constant temperature and humidity chambers, etc. |
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Analytical method development/validation/confirmation/method transfer |
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Raw material release, drug release, and drug stability studies |
