Toxicological Risk Assessment

Toxicological-Assessment-Cosmetics- Pharmaceuticals-Medical-Devices-Chemicals
  • Expertise in EU Reg No 1223/2009 and the Modernization of Cosmetics Regulation Act (MoCRA) of the United States

  • Preparation of Cosmetic Product Safety Reports (CPSRs)

  • Preparation and upgradation of toxicological write-ups for individual ingredients

  • Use of state-of-the-art methodologies and the latest scientific knowledge

  • Evaluation of potential risks associated with products, including exposure assessments and hazard identification

  • Partnership to ensure product safety and conformance with applicable regulations

  • Derive health-based exposure limits (PDE and OEL)

  • Toxicological evaluation of Impurities and Excipients

  • Facilitate toxicology study placement (CRO identification, study design and monitor)

  • Execution of nonclinical safety assessment strategies across various therapeutic areas

  • Preparation of preclinical documents for regulatory submission (IND/CTA)

  • Help derive the maximum recommended starting dose (MRSD)

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