The implementation rules for NMPA (National Medical Products Administration) certification technical support in China provide guidelines and requirements for organizations involved in supporting the certification process of medical devices. These rules outline the responsibilities, qualifications, and procedures that technical support entities must adhere to when assisting manufacturers with NMPA certification. Here are some key aspects typically covered in these rules:

1. Qualifications of Technical Support Entities:

   • Technical support entities must be legally registered entities in China with the necessary expertise and qualifications in medical device regulations and certification processes.
   • They should have a team of professionals with knowledge of relevant technical standards, testing methods, and regulatory requirements.

2. Roles and Responsibilities:

   • Application Preparation: Assist manufacturers in preparing and compiling application materials required for NMPA certification.
   • Technical Documentation Review: Review and verify the completeness and accuracy of technical documentation submitted by manufacturers.
   • Testing Coordination: Coordinate and facilitate testing activities required for demonstrating compliance with Chinese technical standards and safety requirements.
   • Clinical Evaluation Support: Provide support in conducting clinical evaluations or trials, if applicable, including study design, patient recruitment, and data analysis.
   • Regulatory Pathway Guidance: Guide manufacturers in selecting the appropriate regulatory pathway (standard review, special review, expedited review) based on device classification and intended use.

3. Quality Management System (QMS) Requirements:

   • Technical support entities must maintain a robust QMS that complies with relevant standards, such as ISO 13485 or equivalent, to ensure the quality and reliability of their services.
   • QMS should cover document control, record keeping, internal audits, and corrective and preventive actions (CAPA) to support regulatory compliance.

4. Confidentiality and Data Security:

   • Ensure confidentiality of proprietary information and sensitive data provided by manufacturers during the certification process.
   • Implement measures to safeguard data integrity and prevent unauthorized access or disclosure of confidential information.

5. Communication and Reporting:

   • Maintain clear and transparent communication with manufacturers throughout the certification process, providing updates on progress, regulatory requirements, and any issues that may arise.
   • Prepare and submit comprehensive reports to manufacturers and regulatory authorities as required, documenting the outcomes of technical support activities.

6. Continuous Improvement:

   • Implement mechanisms for continuous improvement of technical support services, including feedback mechanisms from manufacturers and updates to knowledge and expertise in evolving regulatory requirements.

These implementation rules aim to ensure consistency, reliability, and efficiency in the support provided to manufacturers seeking NMPA certification for their medical devices in China. Manufacturers should engage with qualified technical support entities that adhere to these rules to enhance their chances of successful certification and market entry.

Whatsapp：+86 15816864648；企业邮箱：htio.lin@grzan.cn