Dissolution Tests are conducted to determine the drug release patterns, physiological availability and bioavailability of formulated drug products. It is also used as a quality control tool.
The Dissolution rate of a drug from the solid state is defined as the amount of drug substance that goes into solution per unit time under standardized conditions of liquid / solid interface, temperature, and solvent composition.
LABINDIA brings to you the State - of - the - art Dissolution Testing apparatus in elegant design with advance features, which supports USP 1,2, 5, & 6. Apparatus for intrinsic test & stationery basket methods are available.
This product is designed on the basis of specifications recommended by international regulatory bodies and the future needs of pharmaceutical industry. The unit can be used to analyze dissolution profile of tablets, capsules etc. as per USP, BP, IP specifications.