Athreva has regulatory experts who can help you to become a trusted and valued  cosmetic manufacturer. With our Safety Assessment, you will:

  • Ensure that your ingredient has been assessed in line with Specific country guidance and legislation
  • Make sure that the information being circulated about your ingredient is accurate and well presented
EU Medical Device Regulation


Risk Assessment

Our experts offer different types of service as required by various cosmetic legislations:


  • Good Manufacturing Practice (GMP)
  • Cosmetic safety assessments to the EU, US, Canada, Saudi Arabia, Australia
  • Preparation and assessment of cosmetic data
  • International Nomenclature Cosmetic Ingredient (INCI) Ingredient labelling
  • Safety assessment report (SAR), Cosmetic Product Safety Report (CPSR), Toxicological Risk Assessment (TRA)
  • Preparation and review of CPSR with credentials (qualified safety Assessor)
  • Consultation for finished products regarding clinical safety studies.
  • Suggestion for any safety test to be conducted, before placing into the market. This suggestion will be based on safety data available and ingredient tox profiles.
  • Toxicology risk assessment report and exposure calculations to determine (MoS) for finished cosmetic product ingredients
  • Preparation of CPSR as per Europe regulation 1223/2009
  • SDS authoring services as per standard format of Globally Harmonized System (GHS)

Legal Representative

Toxicological Assessment


Our regulatory experts and toxicologists take charge of all or part of your international compliance procedures

  • Preparation of general toxicological reports for ingredients
  • Pre-assessment report - Preparation of toxicology reports for cosmetic ingredients
  • Dosage of certain ingredients such as restricted preservatives
  • Guidance on cosmetic testing (stability, microbiology, safety, efficacy)
  • Guidance and support on serious undesirable effects and undesirable effects



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