15 May 2025
The SevenExcellence S400 by Mettler Toledo is routinely used in QC of liquid drug products, where pH is a critical parameter for batch release. The implementation of this Device Driver was realised in version 4m, and is now standard in q-doc.
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08 May 2025
The new DataLink™ SQL Export add-on for q-doc® allows the seamless exchange of data with enterprise data management systems, whether a LIMS, MES or ERP, through standardized database export functions.
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24 April 2025
Whether for demanding analytical laboratory applications or for supplying dishwashers or autoclaves, SOTAX offers a Pure Water System to meet your demands.
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11 April 2025
This week marked a major milestone for us – and we couldn’t be more proud. With two exclusive launch events, we officially introduced JetX™ to the world: Tuesday in Braunschweig and Thursday in Frankfurt.
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03 April 2025
Tapped Density is a valuable tool for evaluating powder quality, as well as flowability & compressibility. The new q-doc® process driver offers enhanced reproducibility & paperless documentation of test results, ensuring reliability & data integrity.
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31 March 2025
Teamwork, skills, and passion – these are key values in both sports and business. That’s why we are excited to support the nine (9) local unihockey (floorball) teams of Reinacher SV in Switzerland.
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27 March 2025
The new SOTAX SDT-L is a compact, space-efficient comparative dissolution tester with 14 vessels designed for simultaneously testing two formulations with a single instrument under 100% identical conditions in GMP environments.
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03 March 2025
SOTAX is proud to officially introduce JetX™ – an innovative solution for Sample Preparation. This new technology allows analysts to achieve 4x more productivity with 80% less effort, all while delivering the same reliable analytical results.
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27 February 2025
This webinar offers a unique opportunity to gain comprehensive insights from multiple perspectives: excipient expertise, analytical testing, and formulation development.
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20 February 2025
In pharmaceutical development, low-volume dissolution testing is essential for evaluating drug release under limited sample conditions, particularly in research involving highly potent compounds, low-dose formulations, and limited API applications.
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