Pharmaceutical Analysis Contract Services

BASi scientists can provide support for all phases of your drug development, from early stage API method development to post-commercialization product testing. Our testing is completed in compliance with all appropriate regulations (cGMP, GLP), and we welcome projects which are analytically challenging. We believe strong lines of communication between our business and yours are essential to the successful completion of projects, and we will customize our approach to meet your unique demands. From your initial inquiry to the final report, BASi will be with you each step of the way.

Pharmaceutical Analysis Services include:

Drug Development Services

• NDA, IND and QC stability program support
• Method development and validation
• Forced degradation studies
• Final product release testing
• Comparator testing
• Dosing solution analysis
• Compendial testing
• Formulation development support
• Stability storage on site
• In Vitro bioequivalence

Dosage Forms Analyzed

• Solids, API, capsules, tablets
• Liquids
• Semi-solids, suspensions
• Drug-coated medical devices
• Transdermal patches
• Cytotoxic and potent materials
• Controlled substances (Schedule 1 - 5)