GMP-Compliant Systems-Zhejiang Tianfu Technology Co., Ltd.

Accurate information empowers, documents drive value: Zhejiang Tianfu Technology's document team's professionalism and perseverance

At Zhejiang Tianfu Technology Co., Ltd., we understand that in the rigorous chemical and pharmaceutical fields, accurate, standardized, and user-friendly technical data and project documentation are as important as the products themselves. They are the critical bridge that transforms technological advantages into customer value and the "nerve center" that ensures efficient project execution and safe operations. Our data and documentation team is the builder and guardian of this bridge, dedicated to ensuring that every piece of information is clear, accurate, and creates value.

Professionalism, system, and efficiency: our core service capabilities

File customization

Audit

Approve

Document
issuance

Training

Effective

Failure

Document
archive

Regular
review

Zhejiang Tianfu Technology has formed a complete set of verification system documents based on the basic verification documents as the premise and support.

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Basic files for verification

The basic files include pressure vessels, atmospheric pressure equipment and pipeline welding, etc.

Pressure vessels: vessel information, task book, material list, blueprint, product quality certificate, main component material list, calculation book, nameplate, cover, equipment parts list and parts random manual compilation, equipment instructions, equipment certificate, equipment operating procedures, etc.

Normal pressure equipment: material list, white drawing, steel plate and head material list, equipment manual, cover, equipment parts list and manual, equipment certificate, equipment thickness test, normal pressure container water leak test, equipment stirring test, 3D dead angle test, equipment roughness test, etc.

Pipeline welding: weld spot diagram, welding records, printed paper, pipeline pickling and passivation, welder qualification certificate, endoscopic inspection records, endoscopic pictures and videos, etc.

Tianfu's verification system document content usually accompanies the entire equipment verification work life cycle.

The key part is carried out through GMP certification document management, including design qualification (DQ), factory acceptance test (FAT), site acceptance test (SAT), installation qualification (IQ), and operation qualification (OQ).

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Basic files for verification

Customer-centered information service concept

Choosing Zhejiang Tianfu Technology means you receive not only first-class products and solutions, but also a complete, accurate, and efficient information delivery system. Our documentation team is a silent yet crucial force in your project.
If you have any technical documentation writing, management, or standardization needs, please contact us. The Zhejiang Tianfu Technology documentation team is committed to professionally ensuring your success.