Advanced Compact Validatable Process Easy Maintenance Mqa Pulsed-Vacuum Autoclave for Medical Workshops

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 equipment uses saturated steam as the sterilizing medium with repeated vacuum-pumping and steam-injection cycles to eliminate residual air, optimizing steam contact and penetration for uniform performance.

Yes, the door is listed as customizable. The standard design features a motor-driven hinged door with automatic opening and closing capabilities.