【CODEX】药品生产监督管理办法（3-4）-EN
Chapter III License Management of Drug Manufacturing
Article 13. A drug manufacturing license has an original and a duplicate, both of which have the same legal effect and are valid for five years.
The drug manufacturing license is formulated uniformly by the CFDA.
Article 14. Items such as license number, name of enterprise, legal representative, person in charge of enterprise, enterprise types, registered address, manufacturing address, manufacturing scope, certificate issuing authority, date of issue and expiry date shall be clearly indicated on the drug manufacturing license. License items which are approved by the food and drug regulatory authorities shall be the person in charge of enterprise, manufacturing scope and manufacturing address.
