Latest updates on our factory and new products

In GMP sterile manufacturing, every small protective consumable forms an important line of defense for workshop compliance control. Compliance management in sterile cleanrooms never relies on a single piece of equipment. Instead, it is implemented through every detail, every consumable and every protection control procedure. As core personal protective equipment worn by personnel, the compliance, stability and traceability of goggles directly affect cleanroom classification and GMP audit outcomes.

During GMP sterile pharmaceutical production, the compliance, stability and traceability of personal protective equipment are key items for daily cleanroom operation and on-site audits. Conventional goggles commonly suffer from easily falling-off markings, lack of sterilization traceability, fog-prone lenses, and dirt accumulation inside vent structures, which have long been weak points for pharmaceutical enterprises in GMP compliance.

To address these common industry pain points, our series of pharmaceutical-grade sterilizable goggles has undergone comprehensive iteration and upgrading. The product line includes three types: disposable, reusable vented, and reusable non-vented goggles. They meet the demands of different cleanroom classes and working scenarios, balancing compliance, practicality and durability to fully satisfy the standardized protection requirements of sterile cleanrooms.

1.Non-vented compliant structure, compatible with the latest GMP cleanroom standards

2.Permanently engraved codes on the body to enable full-lifecycle traceability of the equipment

3.Resistant to moist heat sterilization for multiple reuse cycles

4.Long-lasting anti-fog lenses to maintain clear vision during sterile operations

5.Ergonomic design for comfortable long-duration wear without fatigue

A leading biotech enterprise BeiGene completed the on-site audit of our cleanroom and production workshop. Our production environment, quality control system and sterile packaging products have passed the strict review by the customer’s QA team. We will continue to strictly comply with ISO 15378 and GMP requirements to provide reliable primary pharmaceutical packaging solutions for biopharmaceutical customers.

This audit serves not only as a comprehensive inspection of our quality management system, but also recognition of our quality management capability and overall strength. We will continuously strengthen the development of our quality management system to deliver higher-quality products and services to customers.

Moving forward, we will continue to uphold the philosophy of "Quality First, Customer Oriented". We will steadily improve the effectiveness and adaptability of our quality management system, contributing to the long-term development and continuous innovation of our company.