Bioanalytical Services

A True Partner in BioAnalysis

BiomarkersEurofins 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