Obtaining NMPA (National Medical Products Administration) registration certificate for multi-parameter monitors in China involves a structured process that includes several key steps:

Step 1: Determine Device Classification

1. Device Classification: Determine the classification of your multi-parameter monitor according to NMPA regulations (Class I, II, or III). This classification determines the regulatory pathway and specific requirements for certification.

Step 2: Prepare Technical Documentation

1. Technical File Preparation: Compile comprehensive technical documentation, including:
   • Device description, specifications, and intended use.
   • Design drawings, diagrams, and manufacturing processes.
   • Risk management file, including hazard analysis and risk control measures.
   • Verification and validation data demonstrating device performance and safety.
   • Clinical evaluation data (if applicable).
   • Labeling and instructions for use in Chinese.
   • Software information and validation (if applicable).

Step 3: Quality Management System (QMS) Compliance

1. QMS Implementation: Implement a quality management system that complies with ISO 13485 or an equivalent standard. Ensure your manufacturing processes meet Good Manufacturing Practice (GMP) requirements.

Step 4: Conduct Required Testing

1. Testing Requirements: Conduct testing according to applicable Chinese National Standards (GB standards) or internationally recognized standards. This typically includes:
   • Electrical safety testing.
   • Performance testing (accuracy, reliability).
   • Electromagnetic compatibility (EMC) testing.
   • Biocompatibility testing (if applicable).

Step 5: Clinical Evaluation (if required)

1. Clinical Trials: For higher-risk devices, conduct clinical trials in China to demonstrate safety and efficacy, if required by NMPA regulations.

Step 6: Prepare and Submit Application

1. Application Preparation: Compile all required documentation, test reports, and QMS certificates into a complete application package.

2. Submission: Submit your application through the NMPA’s online portal or via a registered local agent. Include a detailed summary of the device, supporting documentation, and evidence of testing and compliance.

Step 7: NMPA Review and Inspection

1. Review Process: The NMPA will review your application, technical documentation, and test reports. They may conduct on-site inspections of your manufacturing facility to ensure compliance with regulatory requirements.

2. Evaluation: If your application meets all requirements and passes review, the NMPA will issue the registration certificate for your multi-parameter monitor.

Step 8: Post-Certification Activities

1. Post-Market Surveillance: Implement a post-market surveillance system to monitor the performance of your multi-parameter monitor in the market. This includes handling complaints, reporting adverse events, and maintaining device safety and efficacy.

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