Datagov Opendata Platform

The GMP certificate is based on Article 56 of the Pharmaceutical Affairs Law. When a manufacturer intends to export drugs abroad, they must apply for a GMP certificate in accordance with the requirements of the importing country. The GMP certificate is divided into three categories: active pharmaceutical ingredients, API manufacturing facilities, and drug manufacturing facilities (including storage and packaging facilities). This dataset is a list of revoked GMP drug manufacturers, and is simultaneously updated on the website to provide further information for consumers, businesses, and healthcare professionals.