A manufacturer is obliged to provide a full set of documents in accordance with the requirements and standards of the local regulatory body.
The generalized list of documents for consumer healthcare products registration is as follows: - FSC - Free Sale Certificate - COA - Certificate of Analysis - COC - Certificate of Composition (ingredient list with % and function of each ingredient) - Artwork (indicating the country of origin ("Made in...") and a 16-digit barcode on the artwork) - GMP or ISO - Halal certificates (see section “Halal certificates” for more information)