19 September 2023
Save time & money with your supplier audits.
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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News
07 September 2023
AutoCompliance™ reduces costs.
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
Particle Size Distribution vs. Data Integrity?
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
Challenges in comparing breaking force test results.
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
Catching the sun over Aesch, Switzerland.
SOTAX is becoming more sustainable – thanks to the new photovoltaic system at its headquarters.
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20 July 2023
Accelerated In-Vitro Release?
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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17 July 2023
Xtend™: Export PDF reports to USB flash drive or to the EasyTouch™ file share
When operating your Xtend™ dissolution system without q-doc® or WinSOTAX® plus, you can also export reports as PDF.
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29 June 2023
We are SOTAX – since 1973.
The heart of every company is its employees and their contributions. Today, we want to introduce you to just a few of the faces worldwide who make up the SOTAX brand.
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22 June 2023
Are you working with complex dosage forms?
Emerging formulations and novel drug delivery technologies require a revised approach to in-vitro drug release testing. Due to the complex nature of these formulations, extensive testing and development are crucial to ensure patient safety and efficacy.
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25 May 2023
q-doc® – New version 4L available now.
From configurable process drivers to the integration of new testing instruments – the latest software version offers a whole package of new features to make your IPC processes easier and more compliant.
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