01 May 2023
On 01 May 2023, the United States Pharmacopeia (USP) has introduced a new formulation of their prednisone tablets. Make sure to use this new 'Dissolution Performance Verification Standard' (DPVS) for your performance verification tests (PVT).
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03 April 2023
We are happy to announce that SOTAX has been successully audited according to ISO 9001:2015 certification of quality management systems. After having recently added new SOTAX sites to our organization, we proud of our re-certified global quality system.
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28 March 2023
3D printing has opened up new opportunities and possibilities in many areas, including the development and manufacturing of pharmaceutical dosage forms.
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16 February 2023
When it comes to OOS incidents, full traceability is essential. Visual inspection helps to precisely locate the source of the error and robust video monitoring can continue even when the automated process is unobserved on site.
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02 February 2023
With employment rates up and a historically high percentage of vacant jobs, automating your dissolution and sample preparation processes increases efficiency, improves traceability, and allows your lab personnel to focus on mission-critical activities.
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01 January 2023
SOTAX was established in 1973 and over the past 50 years, we have grown from a small regional business to a world-class global organization. Reason enough to celebrate!
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20 December 2022
As the year comes to an end, we would like to take this moment to review the past twelve months briefly and give a brief preview of what awaits us in the New Year.
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08 December 2022
Semi-solids, such as suspensions, creams, lotions, pastes, and gels, can pose problems to analytical method developers and analysts. Automating the required preparation steps with an APW workstation overcomes typical problems of manual preparation.
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22 November 2022
Did you know that you can collect data from Non-SOTAX instruments with q-doc® software? Standard drivers for balances, loss on drying (LOD), refraction, and other type of tests are readily available.
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03 November 2022
Recording the disintegration time of dosage forms such as hard-gelatine capsules can be challenging. Remaining residue (e.g. the empty capsule shell) makes it difficult to reliably determine the end-point for disintegration.
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