Site Licensing

The site licensing system requires that all manufacturers, packagers, labellers, and importers be licensed. Sites must have procedures in place for distribution records and product recalls and for the handling, storage and delivery of their products. They must also demonstrate that they meet good manufacturing practice requirements.

Good Manufacturing Practices for Natural and Non-prescription Health Products

Good Manufacturing Practices (GMPs) must be employed to ensure product safety and quality. They require: appropriate standards and practices regarding product manufacture, storage, handling and distribution of natural and non-prescription health products (NNHPs). For Natural and Non-prescription Health Products, the provisions cover:

  • specifications (product)
  • premises
  • equipment
  • personnel
  • sanitation program
  • operations
  • quality assurance
  • stability
  • records
  • sterile products
  • lot or batch samples, and
  • recall reporting.

The GMPs are designed to be outcome based, ensuring safe and high quality products while giving manufacturers, packagers, labellers, importers and distributors of NNHPs the flexibility to implement quality systems appropriate for their product lines and businesses.

Additional Resources

Report a problem or mistake on this page
Please select all that apply:

Thank you for your help!

You will not receive a reply. For enquiries, contact us.

Date modified: