Our pharmaceutical laboratory provides testing of quality, potency and/or quality compliance of raw materials, intermediates and final products for the pharmaceutical industry in the GMP mode.

The laboratory is ISO 17025 accredited, we have been granted the Decision for Marketing Authorization (issued by State Institute for Drug Control) and we are also FDA approved.

Thanks to our highly qualified and experienced staff, modern analytical instruments and specially secured systems, we can process the orders quickly and effectively. Precision and accuracy of the results is always our top priority.

Our methodologies refer to:

• Ph. Eur. - European Pharmacopoeia
• USP - United States Pharmacopoeia
• CL - Czech Pharmacopoeia
• BP - British Pharmacopoeia
• ICH Guidelines

ALS is always ready to offer International Standards and in-house methods as well as customer specific methods as required.