In order to implement the Drug Administration Law and the Measures for the Supervision and Administration of Drug Production, guide pharmaceutical packaging material production enterprises to standardize their production behavior, and guide drug marketing authorization holders to fulfill their responsibilities of auditing pharmaceutical packaging material suppliers, the National Medical Products Administration has organized the drafting of the "Regulations on the Quality Management of Pharmaceutical Packaging Material Production" (draft for soliciting opinions), which is now open for public comment. Please provide relevant feedback via email before July 2, 2022 ypjgs@nmpa.gov.cn Please indicate "Feedback on Quality Management Standards for Drug Packaging Materials Production" in the email subject.