User Guide

Areas of Work

• Design, conduct, and reporting of Phase I clinical trials
• Consultation for Phase II–III clinical trials
• Consultation for bridging studies
• Pharmacokinetic/pharmacodynamic modeling
• Clinical trial simulation (Computer Aided Clinical Trial, Virtual Clinical Trial)
• Clinical pharmacology study consultation, including bioavailability, formulation, and drug interactions
• Adverse drug reaction consultation, and PROMASYS management and coding
• Consultation and conduct of bioequivalence studies

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