Services
Prepare nonclinical data for first in human clinical studies
Pharmacology
Review of existing data
Conduct gap analysis, select CRO and place studies
Monitor studies and review of CRO reports
Write pharmacology report (internal data) for submission
Summaries and tables for regulatory submission
Pharmacokinetics, ADME
Design, monitor and review of PK and ADME studies
Organize and share data for PK analysis/modeling
Summaries and tables for regulatory submission
Toxicology
Provide consulting and strategic advice
Select CROs and place studies
Monitor studies and review CRO reports
Present and interpret data
Summaries and tables for regulatory submission
Assess risk profile and recommended human dose