• Identifies which SFDA regulatory sector (Drugs, Medical Devices, Cosmetics, etc.) oversees your product
  • Determines whether you need to follow a full registration process, a notification, or if it’s exempt
  • Guides you on what documents, testing, and procedures are required for registration
  • Following the wrong regulatory path
  • Delays in approval
  • Additional costs or re-submissions
  • Product Classification Requests: We’ll submit your product for an official classification through the SFDA system to determine the correct regulatory sector.
  • Clear Guidance: Once classified, we help you understand the next steps and ensure you’re following the right procedures for registration.
  • Expert Support: We provide ongoing advice and assistance to streamline the process and minimize delays.