On November 17, 2022, the Saudi Food and Drug Authority issued a notice to revise the registration principles of enterprises producing health products. Main Contents:

(1) Relevant definitions. The factory and sales certificate of health care products and their products;

(2) Registration requirements. Certificate issued by the regulatory authority of the country of origin, good manufacturing practices, official regulatory materials, company name and address;

The following documents should be submitted in the application for renewal of factory registration: the certificate issued by the competent authorities of the country of origin six months before the end of registration, the regulatory standards of good manufacturing practices, official regular supervision and inspection, etc.

The revision will take effect as of the date of publication.