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1) |
Development of Bioanalytical Methods : LC-MS/MS, GC/MS, HPLC, GC |
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2) |
Bioanalytical Method Validation |
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3) |
Clinical Studies : Determination of Drug Contents in Biological Matrices |
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4) |
Bioequivalence Studies : Determination of Drug Contents in Biological Matrices |
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5) |
TK Studies : Determination of Drug Contents in Biological Matrices of Animals |
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Drug Product Stability Tests
(Long-Term Storage Testing, Stress Testing, Accelerated Testing, Photo Stability Testing) |
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2) |
Specification and Quality Test of Drug Substance |
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3) |
Drug Substance Stability Tests |
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4) |
Quantification of Drug Substance in Dosing Solution |
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5) |
Compatibility Test |
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Test Items :
Dissolution Test, Quantification of Drug Component, Related Impurity Content, Water Content, Hardness, Color and Other Properties |
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1) |
Structure determination of metabolites produced by in vitro metabolic experiment |
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2) |
Structure determination of in vivo metabolites in phase I clinical study |
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3) |
Structure determination of in vivo metabolites in toxicological study |
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4) |
Metabolome research of biomarker relating pharmacology and toxicology |
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5) |
Contract study on proteome |
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1) |
Transporter |
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2) |
CYP enzyme of drug metabolism |
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3) |
Nuclear receptor |
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4) |
Breast cancer |
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