Efficiently manage your dissolution and physical testing results in full compliance with 21 CFR part 11 requirements and FDA data integrity guidelines.
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Pioneering and automating high-quality pharmaceutical testing solutions for dissolution, disintegration, hardness and other physical tests of tablets.
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SOTAX dissolution testers are compliant by design. Proven to have the lowest wobble rating in the industry, no adjustments are required with fixed shaft ...
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Manual and automated dissolution testing systems for paddle (USP 2) and basket (USP 1) methods. Different apparatus types and flow-through cells (USP 4).
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Our global team of experts helps pharma companies worldwide in overcoming the various challenges associated with developing & testing pharmaceutical dosage ...
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Address details of the SOTAX headquarters in Europe, North America, and Asia. Click on "Contact us" to find your local sales & service partner.
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Find out more about the SOTAX Group worldwide. From news section, career opportunities, Management, and SOTAX key subsidiaries.
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Automating your dissolution process increases lab efficiency, improves data quality, and eliminates redundant, error prone tasks in your laboratory.
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