In principle, the Standard Customs Clearance Pre-report is transmitted to the importer, the Ministry of Food and Drug Safety, and the Korea Customs Service upon issuance, and the transmitted records cannot be corrected or changed. However, in exceptional cases where the manufacturing batch number stated on the cosmetic product differs from that on the Standard Customs Clearance Pre-report after customs clearance, and a change is required for quality inspection, a change is possible.
Changes to the manufacturing batch number are processed through the 'Korea Pharmaceutical Traders Association (KPTA)' e-civil service.
The documents required for applying for a manufacturing batch number change are as follows. For the most accurate list of required documents, it is best to inquire with the Korea Pharmaceutical Traders Association.
Changes to the manufacturing batch number on the Standard Customs Clearance Pre-report are permitted only in exceptional cases, so the reason for the change must be clearly and specifically explained. Furthermore, even if the change application is approved, there may be an obligation to notify relevant authorities of the changes. Before applying for a change, please be sure to contact the Korea Pharmaceutical Traders Association to confirm the exact procedures and required documents.
To prevent such issues from recurring in the future, it is crucial to accurately verify and record the manufacturing batch number when applying for the Standard Customs Clearance Pre-report. If the manufacturing batch number is inevitably changed, please immediately amend the Standard Customs Clearance Pre-report or notify the relevant authorities to prevent any disadvantages.
Facing difficulties with Korea-related trade or customs clearance?
JGTP provides professional solutions to navigate complex regulations and streamline your business operations in Korea.
Explore JGTP Services