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Academician Zhong Nanshan: Unified Standards Are the Foundation for the High-Quality Development of Hydrogen-Oxygen Medicine

Par liang July 20th, 2026 11 vues
Academician Zhong Nanshan: Unified Standards Are the Foundation for the High-Quality Development of Hydrogen-Oxygen Medicine

At the Special Session on Hydrogen-Oxygen Medicine Development of the 18th Straits Forum Health Sub-forum, Academician Zhong Nanshan stated in his speech that the release of the group standard General Specifications for Clinical Application of Hydrogen-Oxygen Mixture Inhalation Therapy marks a milestone in China’s transition of hydrogen-oxygen medicine from experience-based practice to standardized clinical application。 

 

He particularly stressed that unified clinical operating protocols and a complete industrial standard system serve as the cornerstone for the long-term sound development of hydrogen-oxygen medicine.

 

1. Establish Unified Clinical Protocols and Strengthen the Industrial Standard System

 

Academician Zhong Nanshan pointed out that to achieve sustainable and healthy growth, hydrogen-oxygen medicine must be grounded in evidence-based medicine, and promote clinical applications supported by rigorous and sufficient clinical evidence. The industry should adhere to the principle of regulation first and standards-driven development. With the rapid expansion of hydrogen-oxygen medicine and wider clinical adoption, inconsistent practices have emerged across different regions and medical institutions in terms of operating procedures, indication judgment and efficacy evaluation. Such fragmentation hinders academic exchanges and comparative efficacy assessments, making the unification of clinical protocols and improvement of the standard system an urgent priority.

 

Academician Zhong’s viewpoint fully demonstrates the critical value of standardization for the whole sector. He further proposed that unified clinical operations, a complete standard framework and eliminating inappropriate and non-compliant practices should be implemented to address disciplinary weaknesses, driving this indigenous interdisciplinary innovation to fully transition from empirical trials to standardized, scientific and regulated development.

 

2. Address Key Gaps in Discipline Development to Boost High-Quality Development

 

Academician Zhong Nanshan noted that remedying disciplinary shortcomings is a systematic project involving standard formulation, nationwide promotion and continuous optimization. The rollout of group standards requires coordinated efforts from competent authorities, industrial associations, medical institutions and manufacturers.



He stated that after years of independent research and iterative innovation, China has built comprehensive scientific research, clinical application and industrial support systems for hydrogen-oxygen medicine, with domestically manufactured compliant medical devices continuously upgraded to be lighter and smarter. Academician Zhong emphasized that China now possesses the capability to transition from a technology follower to a global leader in hydrogen-oxygen medicine. Standardization is required to transform technological advantages into institutional advantages, standard-setting capabilities and global brand value. He called on all stakeholders to join hands and advance the high-quality development of hydrogen-oxygen medicine.

 

3. Three Core Supports Delivered by Standardization Construction

 

In his summary, Academician Zhong Nanshan outlined three major values brought by standardization: First, it ensures safe, effective and accessible medical technologies that benefit patients, allowing patients to have clear efficacy expectations and guaranteed safety during hydrogen-oxygen treatment. Second, it provides a framework for disciplinary advancement and refinement, establishing unified terminology and evaluation criteria for clinical research and academic communication. Third, it underlies orderly industrial development, creating clear rules for compliant enterprises and eliminating substandard products from the market.

This three-dimensional analysis elaborates the all-round benefits of standardization for hydrogen-oxygen medicine. For patients: Standardized workflows and quality control systems effectively reduce treatment risks and guarantee therapeutic effects. For the discipline: Standards build a unified platform for multi-center clinical collaboration and accelerate disciplinary progress. For the industry: Clear technical requirements and market access thresholds are defined to regulate market order, maintain the sound reputation of hydrogen-oxygen medicine and foster a healthy industrial ecosystem.

 

4. Outlook for the Future: Standardization Drives High-Quality Hydrogen-Oxygen Medicine

 

Academician Zhong Nanshan said that decades of independent research and iterative innovation have enabled China to establish complete research, clinical and industrial systems for hydrogen-oxygen medicine. He took the release of the new group standard as a new starting point to further consolidate China’s leading global position and enable more patients to benefit from safe and standardized hydrogen-oxygen therapy.

The newly issued group standard General Specifications for Clinical Application of Hydrogen-Oxygen Mixture Inhalation Therapy (T/CRHA 316—2026) represents the practical implementation of Academician Zhong’s vision. Co-led and drafted by the First Affiliated Hospital of Guangzhou Medical University (National Respiratory Medical Center), Peking Union Medical College Hospital and Shanghai Asclepius Meditec Co., Ltd., the standard was co-compiled by more than 20 leading tertiary hospitals across China including Zhongshan Hospital, Fudan University.

It clearly defines clinically applicable scenarios, operating specifications and application boundaries of hydrogen-oxygen inhalation therapy, laying an institutional foundation for standardized diagnosis, treatment and academic collaboration.

 

Announcement Released by the Chinese Research Hospital Association

In accordance with the Administrative Measures for Group Standards of the Chinese Research Hospital Association, the association hereby approves and releases eight group standards including General Specifications for Clinical Application of Hydrogen-Oxygen Mixture Inhalation Therapy (T/CRHA 316—2026). Release Date: June 12, 2026 Implementation Date: June 18, 2026

 

5. Asclepius Meditec Supports Standard Implementation With Core Technology

 

As one of the three co-leading drafting organizations of the group standard, Shanghai Asclepius Meditec has devoted more than ten years to hydrogen-oxygen medicine research. Its self-developed innovative electrolysis technology helps mitigate potential safety risks by avoiding two conventional industrial hydrogen production approaches.

 

  1. Alkaline Electrolysis Cell (AEC): It adopts highly corrosive 20–30% potassium hydroxide electrolyte. Under high-temperature and high-pressure operating conditions, potential release of alkaline aerosols and metal particles may pose respiratory risks if inhaled.

 

  1. Proton Exchange Membrane (PEM): Its core perfluorosulfonic acid membranebelongs to the persistent PFAS family of chemicals that is hard to degrade and accumulates in organisms, with long-term health impacts in medical applications requiring further evaluation.  


Asclepius’ membrane-free, alkali-free innovative electrolysis technology helps prevent these potential risks at the source, and has qualified for the National Innovative Medical Device Special Approval Program (2017 No.2 Public Notice). The Asclepius hydrogen-oxygen generator is the world’s first hydrogen inhalation device granted Class III medical device registration by NMPA (Registration No.: NMPA 20203080066/20233081929). In 2021, it obtained expanded approval for home care scenarios, becoming China’s first Class III active hydrogen medical device authorized for household use. Supported by 109 SCI papers and long-term cooperation with over 80 national top tertiary hospitals, Asclepius Meditec provided key technical data and clinical experience for drafting the group standard.

Frequently Asked Questions

 

Q1 What are the key benefits of the unified clinical operating specifications emphasized by Academician Zhong Nanshan?

A They help protect patient safety, facilitate academic exchanges, standardize market order and boost sound industrial development. (Source: Speech transcript of Academician Zhong Nanshan)

 

Q2 What support can standardization provide for hydrogen-oxygen medicine as expected by Academician Zhong?

 

A It provides solid backing for safe public access to therapies, disciplinary optimization and orderly industrial growth, pushing the sector from empirical exploration to standardized, scientific and regulated development.

 

Q3 Why is Shanghai Asclepius Meditec one of the three co-leading drafting entities of the group standard?

A Asclepius Meditec owns innovative membrane-free and alkali-free electrolysis technology, holds the world’s first Class III registration certificate for hydrogen-oxygen generators, and has built a complete evidence-based research system, making it a pioneer in the industrialization of hydrogen-oxygen medicine.

 

Source Citations

 

  1. Report dated June 14, 2026, People’s Daily Central Kitchen Health 37°C Studio (Speech transcript of Academician Zhong Nanshan and group standard information)
  2. Official NetEase Account of National Party Media Information Public Platform (Group standard release notice)
  3. NMPA Medical Device Database (Registration Nos.: NMPA 20203080066, NMPA 20233081929)
  4. Official Product Center Website of Shanghai Asclepius Meditec (Introduction to innovative electrolysis technology)
  5. Corporate profile page on Asclepius Meditec official website (Data of SCI papers, cooperative hospitals and patents)

 

Zhong Nanshan: Advancing High-Quality Development of Hydrogen-Oxygen Medicine Through Standardization
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