This service allows the classification of products into pharmaceutical, herbal, health, medical device, banned, or not within the Directorate’s responsibilities, based on the active ingredients in the product’s formulation, the pharmaceutical dosage form, and the medical claims shown in the packaging or internal leaflet attached to the application, and its regulatory status in the reference countries.

- Copy of Artwork (outer /inner label and pack insert )

- Catalogue if available

- Copy of composition certificate issued from manufacturer

- Classification/registration certificate in Country of Origin and other reference countries.