Learn more about Evotec's regulated LC/MS bioanalysis capabilities and expertise including:
- High quality service across all phases of pre-clinical and clinical drug development in compliance with GLP and GCP regulations
- More than 25 years of experience to perform LC/MS activities in a regulated environment
- Extensive bioanalytical method development expertise to meet the most demanding and challenging client needs
- Multidisciplinary collaboration enabling integrated solutions to accelerate the drug development process