Our Services
- Population PK/PD model development, analysis, and clinical trial simulations
- Pharmacometric analysis plan development
- Study design, including sparse sampling strategy development
- CRF and protocol design and development
- PK data management and NONMEM® dataset creation
- Real-time data assembly
- Exposure-response evaluations
- Clinical pharmacology and pharmacometric consulting
- Gap analyses
- Clinical pharmacology plan development
- Dose justification support
- Bridging analyses
- Expert review of modeling efforts
- Systematic analyses and pharmacometrics enterprise consulting
- Canonical document development
- Scientific workflow documentation
- Quality management for pharmacometrics
- Instructor-led and web-based training services
- Optimizing the Implementation of Population PK/PD Assessments
- Introduction to Population PK Data Analysis: A Hands-On Course Using NONMEM®
- NONMEM® for Information Managers
- Engineering the Pharmacometrics Enterprise
- Other Customized Courses Upon Request
- Non-compartmental PK and statistical analysis
- Regulatory report preparation and other technical writing services
- Pharmacometric final technical reports
- CSR sections
- Common technical documents
- IND and protocol development support
- Manuscripts describing modeling efforts