How to achieve zero error in drug sorting while improving efficiency
The cold storage adopts the 'goods-to-person' picking method. After receiving the outbound instruction, the system will instruct the shuttle to take out the medicines from the corresponding cargo space and place them on the conveyor line according to the order requirements. The medicine enters the workstation corresponding to the sorting review area through the conveyor line. After the operator confirms the selected quantity, the checkweigher machine verifies the quantity and weight. If there is any problem, the operator can adjust the quantity of medicines in the warehouse management system in time. The whole operation process does not require the operator to enter the cold storage, which greatly reduces the harm to the human body in the low-temperature working environment. After the order is completed, the conveyor will transport the medicines to the packing station for re-inspection. Here, they are labeled and shipped to the delivery tray in time. As the total volume of my country's pharmaceutical economy continues to increase, it is our mission to quickly change the traditional way of circulation and promote the development of modern pharmaceutical logistics. The automation and intelligent construction of the pharmaceutical supply system is imperative. In this development trend, it is expected to help more pharmaceutical customers increase the sorting speed, avoid sorting errors, and bring continuous economic benefits to partners. Statistical evaluation is not only carried out at the order level, but also at the batch and sub-batch level. When completed, a batch will be saved in the database with data based on the order number, batch number, and sub-batch allocation. These allocated data are needed when the subsequent printing evaluations, because at this stage can be filtered and grouped based on these criteria. Therefore, each batch can be uniquely identified. The order number and batch number can be entered manually by the operator. In order to ensure comprehensive quality control, once the parameters are modified, sub-batches are automatically generated.
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