Eurofins competence center in DMPK

Eurofins ADME BIONALYSES is a Contract Research Organization (CRO) with the comprehensive technical expertise and professional management to work with pharmaceutical, chemical, medical device, biotechnology and cosmetic clients. We provide an industry-leading network of specialized skills and methods in preclinical and clinical Research and Development (R&D). In recognition of the challenges you face, we offer our expertise in the fields of pharmacokinetics, metabolism and bioanalysis, encompassing the complete cycle of drug development, as well as the high standards we have built into our Quality Control (QC) and Quality Assurance (QA) systems.

Eurofins ADME BIOANALYSES services span the complete drug development cycle for new chemical entities (NCE), Biologics & generics.

Select below the testing services to have more information:

Method validation

Since its establishment in 1987, Eurofins ADME BIOANALYSES develops, transfers and validates analytical methods for the analysis of xenobiotics in animal and human biological fluids and tissues.

All method validations for drugs and/or metabolites are conducted in compliance with international requirements.

The validation could be full or partial according to your needs.

List of validated bioanalytical methods

The list of validated methods available within the Eurofins Scientific group and our clinical research centers.To get the complete panel of Eurofins services: Quality Control (stability, microbiological, and chemical analysis), Bioassay, Genomic or Central Lab, visit our website: http://www.eurofins.com/pharma-services