##  [China: Registration Service Platform Launch](/mandate/china-registration-service-platform-launch) 

March 30, 2026

The Center for Drug Evaluation under the National Medical Products Administration (NMPA) has launched a new Registration Service Platform to enhance “Internet + government services” for pharmaceutical companies and the public, improving transparency and efficiency in drug registration processes.

### Key Highlights:

- **Policy Focus:**
    - Digital transformation of drug registration services to improve accessibility, efficiency, and transparency.
- **Scope:**
    - Covers the entire drug registration lifecycle, from pre-registration to post-marketing activities.
- **Key Features / Functionalities:**
    - **End-to-End Registration Guidance**: Comprehensive support across pre-registration, clinical trial applications, marketing authorization, post-marketing changes, and re-registration.
    - **Administrative Process Clarity**: Detailed guidance on application acceptance, electronic processing, verification, and certificate issuance.
    - **Expedited Pathway Support**: Information to assist with accelerated approval and market entry processes.
    - **Industry Feedback Mechanism**: Dedicated Administrative Acceptance Mailbox to collect feedback and improve service quality.
    - **Public Education & Transparency**: Provides accessible information on drug review processes, classification systems, and approved innovative and marketed drugs.
    - **Continuous Optimization**: Platform to be regularly updated with enhancements based on user feedback and evolving regulatory needs.
- **Regulatory Goals:**
    - Improve efficiency and quality of drug registration submissions.
    - Enhance communication between regulators, industry, and the public.
    - Support informed decision-making and greater transparency in regulatory processes.



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Source

<https://www.cde.org.cn/main/news/viewInfoCommon/b1c623383b608fcb94f29ae85df4280a>

 

 

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