13 November 2023
APV and USP invite you to another exciting on-site seminar. This two-day course complements the USP course "Fundamentals of Dissolution Testing" and includes one day of practical training in the laboratory.
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01 November 2023
The manual process of recording and reporting defect samples is often inefficient and error-prone. Streamline this process with the new q-doc® Process Driver 'Aspect Control' and store your data and evaluations in one central location.
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12 October 2023
Are you engaged in research or development of classical or novel dosage forms, including MR tablets, implants, or 3D-printed matrices? Learn more with our comprehensive reference guide, featuring 80 recent scientific publications on FTC dissolution.
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28 September 2023
The bulk density of powders and loose materials affects many parameters from formulation to transport of pharmaceutical products. Reliable control of bulk density is essential for your product quality.
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19 September 2023
SOTAX has an ISO9001-2015 certified global management system that is regularly audited by independent authorities, auditing services providers, and customers.
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07 September 2023
An extensive collaborative study conducted by a consortium of pharmaceutical laboratories makes a strong case that SOTAX AutoCompliance™ and mechanical calibration can significantly reduce the costs of regularly qualifying your dissolution instruments.
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24 August 2023
Although analytical sieving is the most common test in IPC labs to determine the particle size distribution of powders and granulates, recording multiple weight measurements and protocolling all steps has remained a complicated and error-prone process.
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10 August 2023
Two measurement principles are described in the US Pharmacopeia <1217>: Constant speed ≤ 3.5mm/s or linear force ≤ 20N/s. But comparability is only guaranteed when tests are performed under identical conditions.
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27 July 2023
SOTAX is becoming more sustainable – thanks to the new photovoltaic system at its headquarters.
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20 July 2023
Establishing an in-vitro / in-vivo correlation is challenging in the development and testing of pharmaceutical formulations. A discrepancy leads to difficulties in accurately predicting how the formulation will behave and perform in the human body.
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