Shiratori Pharmaceutical Co., Ltd. Japanese
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What we can do
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Šé‹Æ•ûj Contract manufacturing
@ œAPIs, intermediates of APIs and functional organic compounds
œFreezed-dry injectable formulations
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2010”N‚Ö‚Ì’§í Practical application and process improvement
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‰ïŽÐŠT—v Development of new routes
@ œSynthesis system
@„¥Focused Beam
@„ Reflectance
@„ Measurement

@„¥Automatic synthesizer:
@„ "ChemiStation"
@„¥Automatic synthesizer
@„¥Microwave (MW)
@„ system
@„¥Preparation system
@„ with an axial
@„ compression column

@„¤Molecular distillation
@@system and precision
@@distillation

œAnalytical equipment
@„¥High Performance Liquid
@„ Chromatography
@„ (HPLC)

@„¥Gas chromatography
@„ (GC) system
@„¥Thermo analytical
@„ equipment
@„¥X ray diffractometer
@„¥Optical rotation
@„ measurement system
@„¤Equipment for structural
@@analysis
œValidation for testing method
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‘gD} Product list
@ œPharmaceuticals, food additives and chemical products
œPharmaceutical intermediates and chemical products/in-house products
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‰ˆŠv Reaction available
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Advanced chemical intermediates
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Validation for testing method

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Shiratori Pharmaceutical carries out validation after reviewing and defining the conditions of analysis to prove that the testing method employed is appropriate. Validation is applied to purity test methods such as HPLC and GC, residual solvent test with head space GC and assay with other equipment.
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