Stalwart Resourceful Manual Override Load Capacity Steam Type Sterilizer for Biomaterial Tasks

Yes, we are a professional manufacturer of pharmaceutical and laboratory sterilizers, integrating R&D, production, and international trade. We warmly welcome on-site factory visits and remote video factory inspections, so you can verify our production capacity and quality control system.

Yes. Our sterilizers are designed and manufactured following GMP guidelines, FDA 21 CFR Part 11 (electronic records & signatures), and other global pharmaceutical regulatory requirements. They are fully suitable for use in GMP-compliant production environments in pharmaceutical factories and laboratories.

Absolutely. We provide complete, audit-ready documentation packages in accordance with pharmaceutical industry practices and GAMP 5 guidelines, including but not limited to design documents, validation documents, SOPs, FAT, SAT, IQ/OQ/PQ, material certificates, calibration records, and other supporting documents. This documentation fully supports your regulatory audits for pharmaceutical and laboratory applications.

The AZQA series is designed for ampoules, vials, tubular glass bottles, injectable packages, and oral liquid products, performing both sterilization and leak detection.

Yes, we offer flexible customization including custom brand selection for pumps and valves, custom loading racks, and customizable procedures to meet different process requirements.