Product Safety & Regulatory

Regulatory Affairs

We develop and implement registration and compliance strategies for the global marketing of products.

  • Creating regulatory documentation assessments that enable unrestricted global product marketing
    • Compile safety and regulatory information from multiple public and private resources
      • HPI, Environment Canada, Canadian Hotlist, Canadian DSL, NDSL, European Health and Safety Commission, China FDA Inventory, PCPC database, Australia OTC AAN, COLIPA
    • Develop Safety Data Sheets
    • Prepare Product Information Files (PIF) and Compliance Information Files (CIF)
    • Report products in VCRP & CSCA
    • Review INCI disclosures
    • Review for all imports into the US
  • Assessing potential restrictions for raw material usage (e.g. carcinogenicity, reproductive toxicology, etc)
    • EMEA, US, Canada, LA, ASIA and US California Proposition 65
  • Coordinating international registrations to allow U.S.-manufactured products to be sold around the world
    • Certificate of Free Sale, Good Manufacturing Certificate, Power of Attorney
    • Confirm various country requirements and authenticate legal documents