Henan Guoqing Environmental Protection Technology Co., Ltd
The all‑membrane process has received regulatory approval from the pharmaceutical industry, and the company is actively expanding its presence in the pharmaceutical ultrapure water market.
Release time:
2026-09-17
Author:
According to industry reports, with the 2025 edition of the Chinese Pharmacopoeia incorporating non‑distillation methods as a compliant approach for preparing water for injection, membrane‑based processes centered on “reverse osmosis plus EDI” are poised to seize significant policy-driven opportunities in the pharmaceutical water sector.
According to industry reports, with the 2025 edition of the Chinese Pharmacopoeia incorporating non‑distillation methods as a compliant approach for preparing water for injection, the all‑membrane process—centered on “reverse osmosis plus EDI”—is poised to seize significant policy opportunities in the pharmaceutical water sector. Compared with traditional distillation, this process offers notable advantages, including lower energy consumption, controllable operating costs, and the elimination of acid–base regeneration, while its green, low‑carbon characteristics align with the national “dual carbon” strategy.
Leveraging its technological expertise in RO and EDI, the company is actively addressing the purified water and water for injection production needs of industries such as pharmaceuticals and medical devices. Its existing portfolio of EDI ultrapure water systems delivers effluent quality that meets relevant pharmaceutical‑grade water standards, enabling the company to provide end-to-end services—from system design to equipment delivery—and supporting the pharmaceutical sector’s transition toward sustainable, green manufacturing.
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