Tablet Dissolution Testing
A dissolution test is a means of identifying and proving the availability of active pharmaceutical ingredient (API) in their delivered form. A dissolution test reﬂects the availability of active substance and allows the prediction of the time for complete release of the material from the dosage form. This test plays an important role in product development, equivalence studies and for product compliance and release decisions. It is vital that the dissolution system provides accurate and reproducible results. All Pharma Test tablet dissolution testing instruments are fully USP and EP compliant. They use our MonoShaft™ tool system and include a full set of vessel and USP Apparatus 2 paddles. A full range of dissolution accessories is also available.
8-Position USP/EP Tablet Dissolution Testing Instrument with Media Addition Station
Dispersion Releaser – Release Apparatus for Nano- and Microformulations
Online automated dissolution testing system with 14+2 position bath.
The new 14+2 station dissolution testing instrument – ideal for comparative studies such as biowaiver tests.
The flexible dissolution bath for constrained bench space requirements.
This 6 station tablet dissolution bath with individual stirring speed control is ideal for R&D purposes.
The compact, 8-station tablet dissolution testing instrument.
The Magnificent Six. All Six Stations in One Line for Optimal Visibility.
The ideal choice for Biowaiver studies and dissolution method development.
"Dual drive" tablet dissolution bath with independant stirring speed control for front and back row.
The simple, low head dissolution testing instrument.
Large volume dissolution testing instrument for pool test applications.