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Verification
The Validation Department of Shandong Zhongda Engineering Technology Co., Ltd. specializes in providing full‑lifecycle validation services for the pharmaceutical industry, covering purified air‑conditioning systems, cleanroom facilities, computerized systems, and clean piping systems.
The validation lifecycle begins with the development and approval of the User Requirements Specification (URS) and encompasses a series of activities throughout the entire lifecycle—design qualification (DQ), engineering and construction phase (QPP), installation qualification (IQ), operational qualification (OQ), and final performance qualification (PQ)—to validate the user requirements.
1. The Full Lifecycle of Verification

2. Validation Documentation System for Cleanrooms and Air Conditioning Systems

3. Computer-Verified File System

4. Provide a comprehensive, standardized validation documentation system.


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Shandong Zhongda Engineering Technology Co., Ltd. adheres to the business philosophy of “integrity as the foundation, quality first, technological innovation, and service above all,” and is committed to providing attentive, customer‑centric services to clients both at home and abroad.
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Customer Service Hotline
Phone:0531-82342627
Address: 32nd Floor, China Resources Building, No. 11111 Jing Shi Road, Lixia District, Jinan City, Shandong Province
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