Preclinical and Toxicological Study Support

At MRIGlobal, we specialize in supporting preclinical and toxicological studies by providing a comprehensive suite of services:

• Non-GMP API Synthesis & Tox Batch Production – Custom synthesis and scalable production for toxicology studies.
• Preclinical Testing Support – Formulation development, dose preparation, dose confirmation analysis, and chemical characterization for in vivo and in vitro studies.
• Bioanalytical Services – Small and large molecule method development, validation, and quantitative analysis to support PK/TK and toxicology studies.
• Pharmaceutical Analysis – GLP and GMP method development, validation, and full characterization of API and drug product.
• Stability Studies – Comprehensive stability programs, including forced degradation and ICH-compliant storage studies.
• cGMP API Manufacturing – Small-scale manufacturing to support early-phase clinical development.
• Repository Services – Secure storage and distribution of test articles, clinical trial materials, and biological samples.
• High-Throughput Screening & Compound Plating – Robotic 96-well plate preparation for screening assays, including in vitro toxicology panels such as Tox21 or ToxCast.

Whether you need toxicology material for your toxicology studies, bioanalysis, or full IND-enabling support, we’re ready to assist!