Panama Cosmetic Product Registration

• Power of Attorney (POA) from the product’s owner, which contained the name and variations of the product to be registered. 
• The POA must be notarised and approved by the Panamanian Consulate or the Seal of the Apostille.
• In the case of medicated items, a qualitative-quantitative formula must be signed by the manufacturing laboratory’s responsible person.
• Finished product specifications: microbiological and physicochemical specifications.
• Studies to see if the product contains biologically derived substances, vitamins, or easily decomposable components to extend the product’s shelf life.
• Documentation to back up the product’s features, such as “hypoallergenic,” “non-irritant,” and “water-resistant,” among others.
• Certificate of Good Practice (GMP) of the manufacturing laboratory, valid for two years from the date of the expedition (unless the document has a different expiration date), issued by the competent authorities of the country of origin and duly legalised by the Apostille Seal or the Panamanian Consulate.
• The appropriate authorities have issued a Certificate of Pharmaceutical Product (CPP original). & apostilled by the Panamanian Consulate or the Seal of the Apostille
• Certificate of Free Sale, also known as a Certificate for Export or a Certificate to Foreign Governments,
• Two (2) samples of the product in each of its versions as it will be commercialised in our country
• Two (2) original product labels or artwork, including the information mentioned above.
• Specifications for the product’s container and a description of the material kind.
• Product life lifespan as determined by the manufacturer’s lab certification

Name of the product’s distributor in Panama.