28 March 2023
3D printed individualized oral dosage forms.
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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News
16 February 2023
Simplified OOS investigations and traceability with video monitoring.
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
Are you struggling with staffing shortages?
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
50 years – Innovating pharmaceutical testing.
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
...and a happy New Year!
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
How to make sample preparation of semi-solids reliable?
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
Paperless Lab – collect data from multiple devices.
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
DT50 – How to deal with non-disintegrating capsule shells?
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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29 September 2022
Generics – Boost your Time to Market.
Are you struggling with deformulation, API characterization and prototypes comparison when developing a generic drug? Outsourcing these time-consuming initial steps to Pharma Services can help you overcome bottlenecks and shortens time to market.
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28 September 2022
Pharma Services celebrates GMP certification for its Indian site.
The SOTAX Group is pleased to confirm that Ortiv-Q3, a SOTAX joint-venture has received FDCA certification of compliance with Good Manufacturing Practice (GMP) for the testing of drugs and raw materials.
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