Category Archives: Yunnan

Policy Analysis and Guidance: Yunnan Province’s Revised Technical Guidelines for Chinese Herbal Medicine Quality Standards

Yunnan Province’s Drug Administration has released a revised version of the “Technical Guidelines for the Quality Standards Research of Chinese Herbal Medicines,” aiming to enhance the quality and safety of traditional herbs, promote innovation, and align with national regulatory standards. This revision reflects Yunnan’s strategic focus on leveraging its unique herbal resources and ethnic medical practices to drive industry modernization and internationalization.

Key Policy Revisions

Emphasis on Unique and Ethnic Characteristics
- Objective: Protect Yunnan’s distinctive herbal advantages and enrich the knowledge base of ethnic medicinal practices.
- Implementation: The revised guidelines provide comprehensive solutions for organizing and summarizing historical and regional medication habits, linking clinical positioning with safety information through real-world data.
Enhanced Operability
- Details: Specific requirements for research objectives, methods, and standards have been added, including detailed guidance on historical literature collection, clinical data collection, and toxicity trial requirements.
- Impact: Facilitates consensus between researchers and regulators, streamlining the standard-setting and revision processes.
Innovation and Technological Integration
- Encouragement: Reduced barriers for researchers and increased emphasis on leveraging new technologies for accurate identification and component analysis.
- Outcome: Aims to establish new local standards or elevate existing ones, supporting the modernization and global reach of Yunnan’s herbal industry.
Environmental and Sustainable Development Focus
- Measures: Emphasizes compliance in sample collection and encourages research samples from cultivation bases to protect ecological resources.

Policy Orientation and Industry Implications
The revised guidelines position Yunnan as a leader in traditional Chinese medicine (TCM) standardization by:

Quality Enhancement: Strengthening safety and efficacy through rigorous research protocols.
Industry Support: Providing clear pathways for standard development and international market access.
Eco-Friendly Practices: Promoting sustainable resource management to ensure long-term supply stability.

Conclusion
Yunnan’s updated framework for herbal medicine standards not only solidifies the province’s role in preserving traditional knowledge but also paves the way for scientific innovation and global competitiveness. Stakeholders in the TCM sector should align with these guidelines to capitalize on Yunnan’s unique ecological and cultural advantages while meeting evolving regulatory expectations.-China Health Reform Pulse

Policy Source: https://mpa.yn.gov.cn/newsite/ZwgkNewsView.aspx?ID=2c531135-46bf-4ad1-b65e-a85c4eea9e64

Policy Analysis and Guidance: Yunnan’s Routine Medical Consumables Delisting Notification

Yunnan Province’s Government Procurement and Tendering Center has issued a notification regarding the delisting of certain medical consumables under the routine listing work for batch 20250305. This move aims to optimize the market by removing products that no longer meet the listing criteria, ensuring quality and supply stability.

Key Policy Highlights

Delisting Criteria
- Basis: Products are delisted based on enterprise applications and supporting documentation.
- Purpose: To maintain high standards for medical consumables and ensure market efficiency.
Product Details
- Example: The notification includes products like the “一次性使用麻醉呼吸管路组件” (Disposable Anesthesia Breathing Circuit Component) manufactured by Henan Tuoren Medical Device Group Co., Ltd.
Contact Information
- Support: Enterprises can contact the medical device procurement department for further inquiries.

Policy Orientation and Industry Implications
The delisting initiative reflects Yunnan’s strategic focus on:

Market Optimization: Removing underperforming or non-compliant products to enhance overall market quality.
Quality Assurance: Ensuring that only products meeting stringent standards remain available.
Transparency: Providing clear communication channels for enterprises regarding listing and delisting processes.

Conclusion
Yunnan’s approach to delisting medical consumables underscores its commitment to maintaining a high-quality and efficient market. This policy supports the reliability of the medical consumables supply chain and ensures healthcare providers have access to essential, quality-assured products. Enterprises should stay informed of these updates to maintain compliance and market access.-China Health Reform Pulse

Policy Source: http://www.ynyyzb.com.cn/detail.html?infoId=25153&CatalogId=3

Policy Analysis and Guidance: Kunming’s Third Batch of Provincial Alliance Drug Volume-Linked Procurement

Kunming City has announced the results of its third batch of provincial alliance drug volume-linked procurement, with the selected drugs scheduled to be available for trading online starting April 1, 2025. This initiative aims to optimize drug procurement processes, reduce costs, and ensure the availability of quality medications through a volume-linked procurement mechanism.

Key Policy Highlights

Online Trading Catalog
- Details: The selected drugs for Kunming’s third batch of provincial alliance volume-linked procurement are detailed in Attachment 1.
- Discontinuation: Previously selected drugs from the same manufacturer and formulation, as well as some products from the first batch of Kunming’s volume-linked procurement, will be discontinued after the new selected drugs are listed.
Implementation Timeline
- Effective Date: Medical institutions and insured retail pharmacies can procure the selected drugs through Yunnan Province’s Medical Security Information Platform starting April 1, 2025.
Sample Registration
- Filing Requirements: Drugs marked as “Requires Filing” in Attachment 1 must complete the basic drug notification and promise filing process.
- Process: Relevant enterprises should complete filing with the Yunnan Provincial Drug Administration as per the displayed announcement and establish distribution relationships in the procurement system.
Procurement and Distribution
- Direct or Entrusted Delivery: Selected drugs can be delivered directly by the selected manufacturer or entrusted to a pharmaceutical distribution company.
- Contract Signing: Medical institutions, manufacturers, and distributors must sign procurement contracts electronically in the procurement system starting now.
System Access
- Account Registration: Relevant enterprises should register for the procurement subsystem as per the 2024 notification.

Policy Orientation and Industry Implications
The implementation of Kunming’s third batch of volume-linked procurement reflects the city’s strategic focus on:

Cost Efficiency: Reducing drug prices through centralized procurement while maintaining quality standards.
Supply Stability: Ensuring the availability of essential medications through a reliable procurement mechanism.
Transparency: Promoting clear contractual agreements and accountability mechanisms.

Conclusion
Kunming’s volume-linked procurement framework sets a benchmark for regional drug management, emphasizing efficiency, quality, and accessibility. Stakeholders, including manufacturers, distributors, and healthcare providers, should align their operations with these guidelines to optimize compliance and patient outcomes.-China Health Reform Pulse

Policy Source: http://www.ynyyzb.com.cn/detail.html?infoId=25178&CatalogId=3