SERVICES

• U.S. and international chemical regulation, registration and review processes (e.g., FIFRA, FFDCA, TSCA, EU Biocides Directive)

• State regulatory affairs (e.g., California’s Proposition 65)

• Sustainability / environmental assessments of technologies and products

• Reduced risk evaluations

• Inert ingredients and food additives

• Consumer & professional product safety evaluations

• Consumer & professional product use/usage research (survey design, analysis and data management for application in quantitative risk analysis)

• Development of novel methods for human health risk assessment (e.g., exposure monitoring data, pharmacokinetics/dynamics, benchmark dose analysis, stochastic modeling)

• Occupational, residential and dietary (food and water) exposure assessment, including multi-pathway, multi-route aggregate and cumulative exposure modeling

• Scientific database design, development, implementation and data management

• Residential and occupational exposure and biological monitoring - study design, field phase oversight, data interpretation and reporting

• Design and approval process for human subject monitoring studies

• Toxicological profile development, hazard identification and dose-response assessment

• Toxicology study design, oversight and report preparation;

• Human exposure and health risk communication (technical non-technical position documents and presentations; in-house workshops)

• Preparation of peer-reviewed journal publications

• Regulatory policy evaluation and impact analysis

• Technical support for task forces / joint ventures

• Representation at regulatory agency meetings

• Presentations to science advisory panels and participation on expert panels

• Litigation technical support / expert witness testimony