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    • Richard C. Pleus, Ph.D.
    • Gretchen M. Bruce, DABT
    • Michael McCabe, Jr., Ph.D
    • David Lehmann, Ph.D.
    • Heidi C. O’Neill, Ph.D.
    • Gavin Bell
    • Kelli R. Hackney
    • Jeremy A. MacMahon, Ph.D.
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  • More
    • Home
    • Services
      • Toxicology
      • Exposure Assessment
      • Litigation Support
      • Odor Analysis
      • Pharmacology
      • Pharmaceutical Components
      • Product Stewardship
      • Risk Communication
      • Regulatory Support
    • Industries
    • OUR STAFF
      • Richard C. Pleus, Ph.D.
      • Gretchen M. Bruce, DABT
      • Michael McCabe, Jr., Ph.D
      • David Lehmann, Ph.D.
      • Heidi C. O’Neill, Ph.D.
      • Gavin Bell
      • Kelli R. Hackney
      • Jeremy A. MacMahon, Ph.D.
    • Thought Leadership
    • About US
    • Careers
Intertox I
  • Home
  • Services
    • Toxicology
    • Exposure Assessment
    • Litigation Support
    • Odor Analysis
    • Pharmacology
    • Pharmaceutical Components
    • Product Stewardship
    • Risk Communication
    • Regulatory Support
  • Industries
  • OUR STAFF
    • Richard C. Pleus, Ph.D.
    • Gretchen M. Bruce, DABT
    • Michael McCabe, Jr., Ph.D
    • David Lehmann, Ph.D.
    • Heidi C. O’Neill, Ph.D.
    • Gavin Bell
    • Kelli R. Hackney
    • Jeremy A. MacMahon, Ph.D.
  • Thought Leadership
  • About US
  • Careers

Regulatory Support

Increased regulatory scrutiny has led to more environmental, occupational, and consumer exposure regulation. Intertox’s significant experience with regulatory teams highlights the importance of scientific expertise in complex evaluations. Toxicology assessments are crucial for product regulatory compliance. Our staff evaluates and communicates scientific evidence precisely to provide a strong foundation for advocacy.

Regulatory Support Services

  

Risk Assessment & Exposure Analysis

  • Quantitative evaluations of human exposure to chemicals.
  • Hazard identification and dose-response assessments.


Regulatory Compliance Review

  • Assistance in compliance with OSHA, EPA, FDA, REACH, and other regulations.
  • Evaluation  of MSDS/SDS documentation and chemical labeling.


Causation Analysis

  • Evaluation of whether a specific exposure caused alleged health effects.
  • Review of medical and occupational history.


Toxicological Profile Development

  • Creation of detailed chemical hazard summaries.
  • Use of  animal, in vitro, and human data.


Scientific Literature Reviews

  • In-depth  analysis of peer-reviewed studies relevant to the case. 


Data Interpretation & Modeling

  • Interpretation of biological monitoring and environmental data.
  • Use of  toxicokinetic modeling or QSAR tools.


Product Defense & Liability Support

  • Support      in defending product formulations and ingredient safety.
  • Guidance      for recalls or adverse event reporting.


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