Regulations on Updating Data on the National Pharmaceutical Database System

I am researching the National Pharmaceutical Database System and have the following question: According to the regulations, how is the data on the National Pharmaceutical Database System updated? I kindly request editorial support.

According to Clause 2, Article 9 of the Regulation on management and use of the National Pharmaceutical Database System issued together with Decision 412/2020/QD-BYT, the regulations on updating data on the National Pharmaceutical Database System are as follows:

- The Drug Administration updates information on drugs when there are changes in drug labels, indications, recalls, adverse drug reactions, and other information related to state management of pharmaceuticals.

- The Departments of Health of provinces and centrally-run cities update information on pharmaceutical businesses; medical examination and treatment facilities when changes occur, issue notifications of drug recalls, and report drug recalls... in accordance with regulations.

- Pharmaceutical businesses update, automatically interlink in real time, the quantities of purchased/sold/disposed, consumed, and recalled drugs... according to the standardized interconnection protocol.

- Medical examination and treatment facilities fully update prescriptions automatically, promptly interfacing from medical examination and treatment facilities to the system following the issued interconnection protocol.

The editorial team informs you.

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