Assessing and mitigating risk with our guidance on adverse event reporting obligations and methodological recommendations

Choosing the appropriate methodologies, statistical techniques and quality control measures to derive meaningful insights from your collected data

Designing scientifically robust studies and protocols with our expertise in study design, statistical analysis, regulatory compliance, and data collection

Leveraging our signal detection and data analysis tools to understand and properly respond to public health impacts of your drug or product

Tapping into our toxicological expertise to develop robust safety assessments to minimize risks for public health and environmental safety

Integrating our time-tested safety reporting intake processes with solutions for databasing and reporting