Validation & Verification

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Over 40 Years Pharmaceutical Biotech Equipment Manufacturer | E CHUNG

Based in Taiwan, E CHUNG MACHINERY CO., since 1975, is a cGMP pharmaceutical biotech equipment supplier. Main products, including Hot Air Sterilizer, Autoclave, Washing Machine, Tunnel Bottle Washing, Drying & Sterilizing Machine, Stills Equipment and Pure Steam Generator, Through Circulation Dryer, Super Mixing Granulator and so forth.

Following cGMP to manufacture and produce in accordance with WHO and FDA principals. Providing equipment IQ & OQ data manual, and all instruments calibrating report correspondence with cGMP. Fully Auto. LVP / Injection / Oral liquid manufacturing equipment, CIP / SIP piping design and solution service provided.

E CHUNG has been offering customers high-quality cGMP Pharmaceutical biotech equipment, both with advanced technology and 46 years of experience in the pharma and biotech equipment industry, E CHUNG ensures each customer's demands are met.

Validation & Verification

Validation Documentations

We provide validation documentations as customer requirements.
Please let us know if you need more documentations except listed below.

Documentations List:

• Design Qualification(DQ)

• Installation Qualification(IQ)

• Operation Qualification(OQ)

• Performance Qualification(PQ)

• Installation Manual(IM)

• Operational Manual(OM)

• Maintenance Manual(MM)

• Factory Acceptance Test(FAT)

• Site Acceptance Test(SAT)

• Quality Control Certificate(QC)

• Factory Inspection Report(FFR)

• Spare Parts List(SPL)

• Layout Drawing

• P & I D drawing(PID)

• Wiring Drawing

• Pipeline Welding Record

• Material Certification(MC)

• Main Component Manual(MCI)

• Main Component List(MCL)

• Specification Parts List(SPL)