HIGHFINE PHARMATECH CO., LTD. is a Sino-foreign joint venture pharmaceutical equipment manufacturer founded in 1992 and based in Haimen City, Nantong, Jiangsu Province, China. For more than three decades the company has concentrated on one problem that sits at the center of every sterile pharmaceutical plant: producing, storing, and distributing water and process fluids that meet pharmacopeial requirements, then integrating that capability with the filling, preparation, and clean-environment equipment around it.
Our Story: From 1992 to Today
The company began as a joint venture built around pharmaceutical water technology and grew by following the same customers from water treatment into liquid preparation, filling, containment, and lyophilization. That progression shaped how Highfine Pharmatech works today: Highfine coordinates system design, fabrication, automation, and commissioning within the agreed project scope.
As stated on the company website, Highfine Pharmatech today operates 6 factories with 500+ employees, including 66 engineers and 52 senior technicians, across a 60,000+ m2 factory area, and has delivered 10,000+ machines installed and commissioned, supported by 100+ R&D patents.
The company's operating principle is stated simply: "Quality is the first and after service is the most important."
What We Manufacture
Highfine Pharmatech supplies process equipment for pharmaceutical water, liquid preparation, and aseptic production:
- Water and steam systems — purified water systems, distilled water and WFI systems, and pure steam generators
- Liquid preparation — automatic liquid preparation systems for syrups, oral liquids, and injectables
- Aseptic filling and forming — BFS (blow-fill-seal) machines, non-PVC soft bag IV production lines, and vial and ampoule filling lines
- Finishing and environment — freeze dryers and cleanrooms
Systems can be supplied as standalone units or as integrated lines, with automation and documentation packages matched to the intended market's regulatory pathway.
Engineering and Quality
Quality control at Highfine Pharmatech follows the company's 3S quality control system — Specialization, Securitization, and Standardization — supported by an in-house QC testing center that verifies materials, fabrication, and finished equipment before shipment.
The company states that it holds EU CE certification, a Chinese pressure vessel manufacturing permission, and ISO9001 quality certification, and that its equipment serves GMP, cGMP, and FDA-regulated production. It also identifies itself as an excellent supplier and a most potential supplier in the Chinese pharmaceutical machinery industry, a famous brand in Jiangsu Province, and a Grade AAA credible company. These are company-stated honors. Certificates available upon request.
For plant engineers and procurement teams, the practical outcome is a design-review and documentation process that can be aligned with USP, EP, or JP expectations for pharmaceutical water and steam, and with the qualification requirements of the target market.
Markets We Serve
Highfine Pharmatech equipment is used in pharmaceutical and biotechnology facilities across Southeast Asia, the Middle East, Africa, Europe, and the Americas, alongside a domestic Chinese customer base. Export projects are supported through documentation packages, installation supervision, and commissioning support.
A Note on Our Registered Name
For clarity in procurement and customs documentation: the company's registered Chinese name is Nantong Haifa Intelligent Technology Co., Ltd. This is the enterprise-registry rendering of the same company. The official English name used in all business, contracts, and correspondence is HIGHFINE PHARMATECH CO., LTD.
Head office and works: No. 379 Zhonghua East Road, Sanchang Industrial Park, Haimen City, Jiangsu Province, China.
Planning a Water or Filling Project?
Whether you are specifying a purified water and WFI train, a pure steam generator, a liquid preparation suite, or a complete aseptic filling line, our engineers can review your user requirement specification and propose a configuration that fits your process and your regulatory market.
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