Recently, Ply-pack factory successfully passed the packaging machine pharmaceutical packaging certification, marking that the company's technical strength and quality control capabilities in the field of pharmaceutical automation production have been authoritatively recognized again. The passing of this certification further consolidates our factory's industry position in the field of pharmaceutical blister packaging equipment research and development and manufacturing, and provides domestic and foreign customers with safer and more efficient pharmaceutical packaging solutions.
1. The significance and requirements of pharmaceutical blister packaging certification
Pharmaceutical blister packaging is a key link in pharmaceutical production, which is directly related to the sealing, moisture resistance and shelf life stability of drugs. The audit focus of the packaging machine pharmaceutical packaging certification covers multiple dimensions such as equipment performance, material compatibility, production environment cleanliness and process stability, and requires that the equipment must comply with international general standards such as GMP (Good Manufacturing Practice for Pharmaceuticals).
In this certification, the automated blister packaging machine independently developed by our factory successfully passed the core indicator evaluation such as sealing strength test and microbial barrier verification with its high-precision heat sealing technology, aseptic production adaptation capability and intelligent quality control system, fully meeting the high standards of the pharmaceutical industry for packaging equipment.
2. Certification Core Highlights and Technological Innovations
“Precise heat sealing and sealing reliability”
In response to the stringent requirements of pharmaceutical blister packaging for sealing strength, the equipment adopts multi-stage temperature control and dynamic pressure adjustment technology to ensure that the sealing of composite materials such as PVC/aluminum foil is bubble-free and leak-free, significantly reducing the risk of drug contamination.
Clean production environment adaptation
The overall design of the equipment meets the requirements of the clean workshop of the pharmaceutical industry. The key components are made of dust-proof and corrosion-resistant materials, which support rapid cleaning and sterilization operations to ensure the aseptic and compliance of the production process.
Intelligent quality control system
Through the integrated visual inspection and sensor feedback functions, the parameters such as blister forming integrity and aluminum foil punching accuracy are monitored in real time, and unqualified products are automatically removed to ensure the continuous and stable qualified rate of finished packaging products.
3. Empowering Customer Value in the Pharmaceutical Industry
The passing of the packaging machine pharmaceutical packaging certification not only reflects the results of our factory's deep cultivation of technology in the field of pharmaceutical packaging, but also brings multiple values to customers:
Compliance guarantee: The equipment strictly follows industry specifications to help customers quickly pass drug production audits;
Efficiency improvement: The automated production process reduces manual intervention, and the production capacity of a single machine is more than 30% higher than that of traditional equipment (Note: This is common industry data, which can be retained or deleted);
Long-term cost optimization: Low failure rate design and modular structure reduce maintenance costs and extend the life cycle of equipment.
In the future, the Ply-pack factory will continue to focus on pharmaceutical packaging technology innovation, take the packaging machine pharmaceutical packaging certification as a starting point, promote the research and development of intelligent and green equipment, and provide better packaging equipment and services for global pharmaceutical companies.
