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API Synthesis
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Process Development of API, Advance Drug Intermediate and Impurities |
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NCE Synthesis
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Custom synthesis of NCEs for Pre-clinical / Clinical Development |
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Bioassay guided fractionation of natural products
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Initial partitioning, Comprehensive fractionation |
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Isolation and characterization of natural products
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Selective isolation of active molecules & reference compounds
Characterization by different spectroscopic techniques
HPTLC chemo profiling and DNA fingerprinting of crude extracts & active fractions |
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Medicinal herbs/Enriched plant extracts
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Procurement of herbs
Supply of active extracts and combined active extracts |
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Peptide Synthesis
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Custom peptide synthesis, purification and characterization |
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Method Devlopment
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An extensive expertise in analytical method development for applications in pharmaceutical and biopharmaceutical products |
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Method Validation
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A well equipped instrument facility to carry out the validation studies(HPLC, GC and others) as per ICH, FDA and other regulatory requirements. |
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Impurity Profiling,
Isolation
&
Characterization
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A separate infrastructure equipped with latest technologies (Prep HPLC, LC-MS etc) to support the high quality of work in Detection, Isolation, Identification and the Characterization of impurities. |
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Stability studies
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A well equipped storage facility includes multiple chambers covering a range of world climatic ICH storage conditions as well as other environmental conditions as per the requirement |
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