Newly revised "Implementing Rules for the Regulations on the Management of Human Genetic Resources" announced
Quick Look
- In accordance with the latest revisions of the Biosafety Law and the Regulations on the Management of Human Genetic Resources, the National Health Commission has revised the "Implementation Rules of the Regulations on the Management of Human Genetic Resources" issued by the former Ministry of Science and Technology in June 2023.
- There are eight chapters and 61 articles.
- It mainly adjusts the regulatory entities, optimizes the approval and filing management system, improves the supervision chain, and ensures the standardized, safe and efficient use of human genetic resources.
AI-generated summary
Why It Matters
In order to thoroughly implement the spirit of party and state institutional reform, in accordance with the latest revisions involving the adjustment of human genetic resources management responsibilities in the "Biosafety Law of the People's Republic of China" and the "Regulations of the People's Republic of China on the Management of Human Genetic Resources", the National Health Commission organized and revised the "Details for the Implementation of the Regulations on the Management of Human Genetic Resources" issued by the former Ministry of Science and Technology in June 2023.
China News Service, November 11. According to the website of the National Health Commission, in order to deeply implement the spirit of party and state institutional reform, in accordance with the latest revisions involving the adjustment of human genetic resources management responsibilities in the "Biosafety Law of the People's Republic of China" and the "Regulations of the People's Republic of China on the Management of Human Genetic Resources", the National Health and Health Commission organized and revised the "Details for the Implementation of the Regulations on the Management of Human Genetic Resources" (hereinafter referred to as the "Details") issued by the former Ministry of Science and Technology in June 2023.
This revision adheres to the overall coordination of development and safety, and aims at "safe management, respecting rights and interests, promoting sharing, and efficient utilization" to effectively protect and rationally utilize my country's human genetic resources, safeguard national biosecurity and social public interests, and promote high-quality development in the field of medicine and health. Revise the higher-level laws and regulations, implement legal responsibilities and reform requirements, mainly adjust the regulatory entities, optimize the approval and filing management system, improve the supervision chain, etc., to ensure the standardized, safe and efficient use of my country's human genetic resources.
The "Detailed Rules" contain eight chapters and sixty-one articles. Chapter 1 General Provisions stipulates the scope of application, relevant definitions, responsibilities of all parties, etc. Chapter 2 Investigation and Registration clarifies the responsibilities of national and provincial authorities, conducts investigations and registration of important genetic pedigrees, and establishes a dynamic list. Chapter 3 Collection of Human Genetic Resources clarifies the collection application conditions, multi-center collection procedures, etc. Chapter 4, Preservation of Human Genetic Resources, clarifies the preservation application conditions, application unit management requirements, etc. Chapter 5 uses human genetic resources to carry out international cooperation, clarifying the application conditions, application rules, cooperative research status reports, changes in matters, etc. for international cooperative scientific research. Chapter 6: The export of human genetic resource materials and the provision or open use of information to the outside world, stipulates declaration rules, simplified procedures, etc. Chapter 7, Service and Supervision, clarifies the regulatory responsibilities, supervision and inspections, emergency and rapid approval systems of competent departments at all levels.
Open Questions
- When will the revised "Details" be officially implemented?
- What are the specific contents of the adjustment of regulatory entities?
- How to operate the simplified procedures for the approval and filing management system?






