Bioanalytical Services
A True Partner in BioAnalysis
Eurofins Medinet has been serving the pharmaceutical industry with high quality, bioanalytical and clinical laboratory services for over 20 years. We offer a wealth of experience to fulfill your analytical needs throughout every phase of drug development, including method development and validation, metabolism and toxicology studies, therapeutic drug monitoring, analysis of clinical trials, and PK/PD studies.
Our number one priority is getting to know our clients and their projects. We take the time to thoroughly discuss our clients’ requirements and know the right questions to ask to help us fully comprehend the basis of every project. This knowledge forms a strong foundation and enables us to develop a highly productive relationship – a true partnership – and, from the very start, you, our client, are at the very heart of our operation.
- Development and validation of analytical methods (according to FDA guidance and Crystal City updates)
- Bioanalysis
- Analysis of drug and metabolite(s) in biological fluids
- Exposure measurement during Tk studies
- Follow up of first in man
- Phase I to III
- Pharmacokinetics
- Calculation and interpretation of Pk parameters
- Statistical analysis
- Therapeutic Drug Monitoring
Laboratory Excellence
Eurofins Medinet is committed to providing the highest quality services; accurate, timely results, and expert advice from our highly qualified team of experienced scientists. Our laboratories are certified to the following quality standards: ISO 15189 – ISO/IEC17025 - OECD Principles of Good Laboratory Practice (OECD GLP), and Good Clinical Practice.
Trust, Experience, Reliability, Integrity, Expertise, Respect, Quality
Scientific poster
Multi-analyte assay of 23 Anti Epileptic Drugs (AEDs) in human plasma
Brochure
Validated methods - Bioanalysis
