Nonclinical Contract Research

We offer a wide range of services from safety, pharmacodynamic, and pharmacokinetic testing for regulatory applications, to exploratory studies in the early stages of research and development as well as consulting services. Our facilities are compliant with GLP (Good Laboratory Practice) for pharmaceuticals, medical devices, regenerative medicine products, agricultural chemicals, Chemical Substances Control Law, and more.

• Safety Studies
• Genotoxicity Studies
• Safety Pharmacology Studies
• Pharmacology Studies
• Pharmacokinetic Studies
• Characterization Studies of Test Substances, Concentration Analysis of Formulations
• Pathological Examination
• Consulting/Advisory Services
• Education and Training
• Medical Writing

Bioanalysis Services

We provide analytical services for drugs, their metabolites, and biomarkers in biological samples. Our team offers comprehensive support including analytical method development and validation as well as measurement of samples, from the basic research/screening stage to the verification/clinical development stage.

• Analytical Method Development and Validation
• Determination of Drug Concentration
• Biomarker Analysis
• Cell Characteristic Analysis
• Genetic Analysis
• Spatial Analysis in Tissue
• Long-term Storage of Bioanalytical Samples (Specimen)

Central Laboratory Services

We perform centralized testing for clinical trial samples from nationwide medical institutions. This avoids any potential platform discrepancies between institutions, as well as unifies testing methodologies and reference ranges. We are also able to address our clients’ drug development needs in terms of globalization through mediford’s global laboratories network.

• Project Management
• Sample Collection Kit Production, Sample Pickup Service
• Clinical Testing, Sample Management
• Reporting of Test Results, Web Browsing System
• Globalization in Drug Development