Line-Link Purification Technology (Shanghai) Co., Ltd
Total Solution For Cleanroom System
Processing Equipment Series
Quality Assurance
★ International lastest technology, configured and aonstructed with high
★specifications, ensure first-class quality
★ Fully in compliance with WHO, FDA, EUGMP, cGMP requirements
★ Experienced R&D team and project management team provide high standard products and service
★ High standard equipment and validation documenation
★ Short lead time and quick response
★ Professional engineering service and validation support
★ Big scale fabrication with high standard, sufficient spare parts supply
★ Professional and efficient after sales service around the world
Documentation & Validation
To provide a full set of documentation for qualification and validation, fully meet the requirements of FDA/EUGMP/WHO/CGMP.
● Project documentation
● Manufacuring documentation(incl.PV/Piping system)
● Control system validation document (FS, HDS, IO List, Wiring Drawings, SDS, SCADA List, PLC software)
● Operational Manuals
● Maintenance Manuals
● Components datasheet
● Design Qualification Protocols
● Performance Qualification support
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