Scantox offers a comprehensive full bioanalytical package of LC-MS/MS method development, validation, and sample analysis for both exploratory and regulatory studies.

Our dedicated team of bioanalytical chemists have long experience in working with regulatory studies and they are experts in LC-MS/MS bioanalytical method development and validation for the quantification of small molecules and peptides within a variety of different matrices.

We have long experience from bespoke method development and validation of bioanalytical methods, not only for small organic compounds but also peptides, and there are few biologic matrixes we have not encountered over the years. 


Scantox is your bioanalytical partner throughout your entire drug development program.

Our instrument set-up consists of LC-MS/MS and GC-MS of different make and model in order to be able to determine the most suitable method for the particular combination of analyte, matrix and LOQ requirement. 

Our bioanalytical team consists of scientifically and technically strong scientists and technicians with a long and deep understanding of LC-MS/MS bioanalysis, and hence the experience and knowledge to guide your assay strategy throughout your drug development program. We set up good, reliable methods, quickly and cost effectively with the customer in focus.

Working according to OECD GLP on non-clinical safety studies we validate our analytical methods in accordance with EMA guidelines for bioanalysis and we take pride in the quality of the results we deliver. We offer sample analysis according to the OECD GLP and additionally according to Good Clinical Practice (GCP) enabling us to move your bioanalytical program all the way from discovery to regulated preclinical studies and beyond into the clinic. Hence, Scantox can be your bioanalytical partner throughout your entire drug development program.

Our instrument park contains 

  • UHPLC-QQQ for trace level determinations and bioanalysis, 
  • UHPLC-DAD-QTOF which gives us the possibility to study degradation substances, extractables/leachables and contaminants, and 
  • GC-MS for volatile substances.  

We also have equipment for batch control/release testing of pharmaceuticals or pharm dev (Dissolution, Disintegration, Blister leak test, TOC, KarlFischer, Subvisible particles. FT-IR etc.)

We are audited for applicable parts of GMP, GLP & GCP


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