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Human Medicines Registration

  • Participating in the process of developing / updating the requirements and regulations for human medicines registration.
  • Reviewing submitted files of human medicines to ensure the quality, effectiveness and safety.
  • Registering human medicines.
  • Reviewing requests for changing the specifications of registered human medicines.
  • Preparing for and conducting regular meetings of the committees responsible of human medicines registration.
  • Documenting and keeping records about all registered human medicines and regularly updating data base.

More Services

Application form

On line Registration