We offer not only technologically advanced analytical equipment, but also a highly experienced team of specialists who are fully committed to every research project.
Thanks to our expertise, we are able to carry out pharmaceutical method transfer, which involves implementing existing analytical methods from other laboratories or pharmaceutical companies into our quality system.
This approach saves time and reduces costs associated with developing and validating new analytical methods.
We also develop new, custom analytical methods tailored to the individual needs of our clients.
Our expertise enables us to design effective, precise and fully validated analytical procedures that ensure accurate testing of active substances and finished pharmaceutical products.
One of our key areas of expertise is the analysis of nitrosamines – a group of chemical compounds subject to strict regulatory monitoring in pharmaceuticals.
Due to their potential mutagenic and carcinogenic effects, we employ highly sensitive LC-MS/MS analytical methods capable of detecting them at trace concentration levels.
We are equipped with an extensive range of analytical instrumentation, enabling us to perform even the most demanding pharmaceutical analyses.
Our core area of expertise is liquid chromatography (HPLC/UHPLC) – a key analytical technique used in pharmaceutical quality control.
It allows for:
quantitative determination of active pharmaceutical ingredients (APIs),
identification of impurities,
assessment of product stability and quality,
analysis of degradation profiles and breakdown products.
All analyses are carried out with the highest level of precision and in full accordance with applicable quality requirements and pharmacopeial regulations.
We ensure full compliance with client specifications, legal requirements and industry standards.
If you need support with pharmaceutical analyses, method transfer or the development of new analytical procedures – feel free to contact us.
