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流池法 USP4法 SOTAX CE7smart

CE 7smart

Flow through cell Dissolution Tester Dissolution tester for poorly soluble and release control dose forms The CE 7smart is the 4th generation of Sotax’s design for dissolution of poorly soluble and release control dosage forms via USP Apparatus 4 (Flow-Through Cell Dissolution), and is compliant to USP, EP and JP for Small Volume Dissolution and Poorly Soluble Compound Testing under

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Library

Library Application Notes Chemspeed Technobis Chemspeed AutoPlant Emulsion Polymerizationson the Chemspeed AutoPlant High Output Ruthenium-Catalyzed Hydrogenation of Hexoses High Throughput Drug Profiling Suspensions, slurry transfers and filtration on the Chemspeed MiniPlant SWING Automated, Microwave Assisted Alkene Synthesis via Wittig Reaction Characterization of Medicinal Plants in Traditional Chinese Medicine (TCM) Utilising the substance handling capability of Chemspeed’s Swing platform for library

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力扬企业 香港力扬 NIKYANG

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Automated Solutions DMSSample bank DMS Sample Bank DMS (Dried Matrix Spot) can collect micro quantity of liquid. Through a piece of DMS card, liquid samples can be collected anywhere and store easily without cool chains. It can be directly analyzed with LC/MS and apply to areas such as diagnosis, pharmacy, food and environmental monitoring to create accurate, low-cost databases. Read

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Pharmaceutical Testing

Pharmaceutical Testing Quality control is indispensable in the pharmaceutical product development process to ensure that the drug substance and other raw materials are suitable for use in your drug product and to ensure that the drug product manufactured meets the quality standards. Quality control is required throughout the entire development process, from drug substance and raw material control, through intermediate

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SOTAX

SOTAX Quality control is indispensable in the pharmaceutical product development process to ensure that the drug substance and other raw materials are suitable for use in your drug product and to ensure that the drug product manufactured meets the quality standards. Quality control is required throughout the entire development process, from drug substance and raw material control, through intermediate drug

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