Company History
Experience
ToxServices Staff
Corporate Social Responsibility
Toxicology and Chemical Risk Assessment
Drinking Water Contaminants and Food Safety
US EPA: Design for the Environment Program and CleanGredients
Product Safety Evaluations
Study Design, Coordination, and Data Analysis
Third Party Audits
Environmental and Sustainability Assessments
Research, Compliance and Expert Witness
Personal Care Products, Cosmetics, and Fragrances
Pharmaceutical/Dietary Supplements/Medical Devices
Drinking Water Industry
Food Industry
Third Party Certifiers
Washington Office
Experience
ToxServices Staff
Corporate Social Responsibility
Toxicology and Chemical Risk Assessment
Drinking Water Contaminants and Food Safety
US EPA: Design for the Environment Program and CleanGredients
Product Safety Evaluations
Study Design, Coordination, and Data Analysis
Third Party Audits
Environmental and Sustainability Assessments
Research, Compliance and Expert Witness
Personal Care Products, Cosmetics, and Fragrances
Pharmaceutical/Dietary Supplements/Medical Devices
Drinking Water Industry
Food Industry
Third Party Certifiers
Washington Office
ToxServices
Corporate Headquarters
1367 Connecticut Avenue NW,
Suite 300
Washington, DC 20036
Telephone: 202-429-8787
Fax: 202-429-8788
Corporate Headquarters
1367 Connecticut Avenue NW,
Suite 300
Washington, DC 20036
Telephone: 202-429-8787
Fax: 202-429-8788
Pharmaceutical/Dietary Supplements/Medical Devices
Evaluate nonclinical data for Investigational Device Exemptions (IDE).
Conduct pre-study audits of toxicology and bioanalytical testing facilities to ensure compliance for Sponsor studies.
Quality assurance review of study design to ensure compliance with FDA Quality System (QS) regulations.
Evaluate the safety of dietary supplements.
Literature review and analysis of toxicology and pharmacokinetic studies to develop occupational exposure limits (OEL).
Conduct pre-study audits of toxicology and bioanalytical testing facilities to ensure compliance for Sponsor studies.
Quality assurance review of study design to ensure compliance with FDA Quality System (QS) regulations.
Evaluate the safety of dietary supplements.
Literature review and analysis of toxicology and pharmacokinetic studies to develop occupational exposure limits (OEL).