For pharmaceutical packaging manufacturers, in order to produce high-quality pharmaceutical packaging with a Class A rate of over 99%, to eliminate the generation of heavy codes, bit errors, and waste codes, in addition to having efficient, stable, and sophisticated signing equipment, The following four aspects of work should also be done in production management.
Safe and stable information flow management
The transmission of electronic supervision code in the production process must be seamlessly connected to ensure its security and uniqueness. It mainly starts from the following three aspects: setting up an electronic supervision code management specialist; establishing a data security delivery process; and developing data security reception. system.
Strict and precise quality control
In the production of code, pharmaceutical packaging manufacturers must monitor the quality from both hardware and software, in order to produce high-quality products, to provide customers with safe, stable and efficient pharmaceutical packaging.
1. Hardware aspects
Firstly, an online quality detecting device is installed on the signing device to detect large products and reject the unqualified products. Secondly, an electronic supervision code detecting device is installed on the testing machine to perform offline detection on the die-cut products one by one. Including the product's code quality and print quality, to ensure that the A-level rate of the coded product reaches 99%, and 100% reach the C-level or above.
2. Software aspects
The software here refers to management. First, a full-time electronic supervision code QC (Quality Control) staff is available. Secondly, after the coded products are made into finished products, the finished product inspectors shall conduct random inspections on the finished products according to national standards.
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Shijiazhuang AoFeiTe Medical Devices Co., Ltd. , https://www.aofit.com