As a GMP accredited and FDA certified contract laboratory in Switzerland, UFAG Laboratorien AG provides Analytical Services for the Pharmaceutical, Biotech, and Medical Device Industries including QC of raw materials/products, method development/validation, stability studies, bioanalytical and biosimilar testing, for small and bio-molecules (e.g. oligonucleotides, mAB).

Our range of services encompasses chemical, physical, physico-chemical and microbiological analyses in accordance with international pharmacopoeias such as the European Pharmacopoeia (Ph. Eur.), the United States Pharmacopoeia (USP) and other pharmacopoeias (BP, JP etc.) We will also integrate and use your analytical testing guidelines as customer methods in our SOP system.

We can provide you with support in the development, optimisation and validation of methods. The scope of the work involved here is oriented along the ICH guidelines or according to your individual wishes. We will be happy to carry out your assignments and projects - we can find solutions even for particularly analytical problems.