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.
This 6 station tablet dissolution bath with individual stirring speed control is ideal for R&D purposes.
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Its 6 vessels, arranged in a single line offer optimal visibility of the dissolution process.
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"Dual drive" tablet dissolution bath with independant stirring speed control for front and back row.
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Offline automated dissolution system with 6 position bath.
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Offline automated dissolution system with 8 position bath.
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Offline automated dissolution system with 6+2 position bath.
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Offline automated dissolution system with 12 position bath.
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The IDS 1000 in-situ dissolution system with fiber optic technology brings direct measurement technology to dissolution testing.
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8-Position USP/EP Tablet Dissolution Testing Instrument with Media Addition Station
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The new 14+2 station dissolution testing instrument – ideal for comparative studies such as biowaiver tests.
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