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Latest Guidebook for Chinese Special Examination and Approval Procedures for Innovative Medical Devices (2019 Edition): speed up overseas innovative medical devices entry into Chinese market

April 2019 | 41 pages | ID: CFA6926C610EN
Access China Management Consulting Ltd.

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SUMMARY

Facing a gigantic population and rapid population aging, China’s regulatory framework for medical devices is undergoing radical changes. In order to promote the implementation of a strategy of healthy China, transform the treating diseases as focal points into the people’s health as centre, prevent and control the major diseases, actively respond to the aging of the population and accelerate the development of aged healthcare service to give the populace with a full range and full-cycle health and medical services for lifetime, the Chinese “National Medical Products Administration (NMPA)” issued the latest modified version of “Special Examination and Approval Procedures for Innovative Medical Devices” on November 2, 2018, and implemented on December 1, 2018. Its aim is to encourage research and innovation of medical devices, promote the popularization and application of new technologies for medical devices to finally meet the growing medical care needs.

Chinese special examination and approval procedures for innovative medical devices established a fast-track approval path and an interactive mechanism between the Chinese drug regulatory authorities and the applicant for innovative medical devices, which reduces risk from the review uncertainty and approval delays that avoid to exhaust applicant's time and energy. This fast-track approval path and an interactive mechanism between the Chinese drug regulatory authorities and the applicant for innovative medical devices offer a huge business opportunity for the foreign medical device manufacturers to achieve a successful entry into Chinese healthcare market and smoothly operate their business in China.

How to grasp the opportunity to speed up your innovative medical device product approval? The overseas and multinational medical device manufacturers must have a comprehensive knowledge of the Chinese special examination and approval procedures for innovative medical devices.The Chinese regulatory approach is unique.

“Latest Guidebook for Chinese Special Examination and Approval Procedures for Innovative Medical Devices (2019 Edition): speed up overseas innovative medical devices entry into Chinese market” provided a comprehensive knowledge of the latest Chinese special examination and approval procedures for innovative medical devices to guide your practical operation how to comply with the Chinese regulations.

The organizations of this guidebook are arranged as follows. Chapter 2 introduces what innovative medical devices are applicable to Chinese special examination and approval procedures. Chapter 3 introduces who are the Chinese regulatory authorities for special examination and approval of overseas innovative medical devices. Chapter 4 elaborates the special regulations for overseas applicant. Chapter 5 introduces how many application dossiers for an oversea innovative medical device should be prepared. Chapter 6 provides the practical guidance for application of special examination and approval procedures of overseas innovative medical devices. Chapter 7 elaborates the benefits from special examination and approval procedures of innovative medical devices: priority processing and interactive mechanism. Chapter 8 conclusions give significant suggestions for overseas and multinational medical device manufacturers to acquire the qualifications of special examination and approval procedures for overseas innovative medical devices. Chapter 9 appendices provide a full set of the English and Chinese bilingual forms relating to the overseas applicant applying for special examination and approval procedures of overseas imported innovative medical device and information communication and exchange of overseas imported innovative medical device with the Chinese drug regulatory authorities, and the feedback letter from the Chinese drug regulatory authorities.

The audiences of this guidebook are overseas medical device manufacturers wishing to enter into the Chinese medical device market, and multinational medical device companies have penetrated into the Chinese medical device market, and their senior executive officers engaging in regulatory affairs expecting to understand how to apply for registration of their medical device products in China and how to comply with the latest Chinese regulations for medical device registration.

After having skimmed through this guidebook, audiences can clearly acquire not only a comprehensive knowledge of the latest Chinese special examination and approval of overseas innovative medical devices but also the practical operation how to comply with the latest Chinese special examination and approval of overseas innovative medical devices. Access China Management Consulting Ltd hopes this guidebook, based on full and accurate regulations, can guide overseas and multinational medical device manufacturers and producers to achieve a successful entry into the Chinese medical device market and smoothly operate their products in China.

REASONS TO BUY

The Chinese “National Medical Products Administration (NMPA)” issued the latest “Special Examination and Approval Procedures for Innovative Medical Devices” on November 2, 2018, and implemented on December 1, 2018. Chinese special examination and approval procedures for innovative medical devices established a fast-track approval path and an interactive mechanism between the Chinese drug regulatory authorities and the applicant for innovative medical devices, which reduces risk from the review uncertainty and approval delays that avoid to exhaust applicant's time and energy. This fast-track approval path and an interactive mechanism between the Chinese drug regulatory authorities and the applicant for innovative medical devices offer a huge business opportunity for the foreign medical device manufacturers to achieve a successful entry into Chinese healthcare market and smoothly operate their business in China. How to grasp the opportunity to speed up your innovative medical device product approval? The overseas and multinational medical device manufacturers must have a comprehensive knowledge of the Chinese special examination and approval procedures for innovative medical devices. The Chinese regulatory approach is unique.

“Latest Guidebook for Chinese Special Examination and Approval Procedures for Innovative Medical Devices (2019 Edition): speed up overseas innovative medical devices entry into Chinese market” provided a comprehensive knowledge of the latest Chinese special examination and approval procedures for innovative medical devices to guide your practical operation how to comply with the Chinese regulations. It is an essential resource for overseas and multinational medical device manufacturers to speed up overseas innovative medical devices entry into Chinese market, which provides not only a comprehensive knowledge of the latest Chinese special examination and approval procedures for innovative medical devices but also the practical operation how comply with the latest Chinese regulations to smoothly navigate complex regulatory requirements.

KEY HIGHLIGHTS
  • What overseas imported innovative medical devices are applicable to Chinese special examination and approval procedures?
  • Who are the Chinese regulatory authorities for special examination and approval of overseas imported innovative medical devices?
  • The Chinese special regulations for overseas applicant.
  • How many application dossiers for special examination and approval procedures of an oversea imported innovative medical device should be prepared?
  • The detailed practical guidance for application of special examination and approval procedures of overseas imported innovative medical devices to smoothly navigate complex regulatory requirements.
  • What are the benefits from Special Examination and Approval of Innovative Medical Devices: Priority Processing and Interactive Mechanism.
  • The significant suggestions for overseas and multinational medical device manufacturers to acquire the qualifications of special examination and approval procedures for overseas imported innovative medical devices.
  • A full set of the English and Chinese bilingual forms relating to the overseas applicant applying for special examination and approval procedures of overseas imported innovative medical device and information communication and exchange of overseas imported innovative medical device with the Chinese drug regulatory authorities, and the feedback letter from the Chinese drug regulatory authorities.
CHAPTER 1 EXECUTIVE SUMMARY

CHAPTER 2 WHAT INNOVATIVE MEDICAL DEVICES ARE APPLICABLE TO CHINESE SPECIAL EXAMINATION AND APPROVAL PROCEDURES

CHAPTER 3 WHO ARE CHINESE REGULATORY AUTHORITIES FOR SPECIAL EXAMINATION AND APPROVAL OF OVERSEAS INNOVATIVE MEDICAL DEVICES

CHAPTER 4 SPECIAL REGULATIONS FOR OVERSEAS APPLICANT

CHAPTER 5 HOW MANY APPLICATION DOSSIERS FOR OVERSEA INNOVATIVE MEDICAL DEVICE SHOULD BE PREPARED

5.1. Content Requirements for Application Materials
5.2. Format Requirements for Application Materials
5.3 Other Special Requirements for Application Materials

CHAPTER 6 PRACTICAL GUIDANCE FOR APPLICATION OF SPECIAL EXAMINATION AND APPROVAL PROCEDURES OF OVERSEAS IMPORTED INNOVATIVE MEDICAL DEVICES

Figure 1 Application Process for Special Examination and Approval Procedures of Overseas Imported Innovative Medical Device
Figure 2 Application Process for Communication and Exchange of Overseas Imported Innovative Medical Device

CHAPTER 7 WHAT ARE THE BENEFITS FROM SPECIAL EXAMINATION AND APPROVAL PROCEDURES OF INNOVATIVE MEDICAL DEVICES: PRIORITY PROCESSING AND INTERACTIVE MECHANISM

Figure 3. Overview of the Benefits of Special Examination and Approval Procedures for Overseas Imported Innovative Medical Devices

CHAPTER 8 CONCLUSION: SINCERE ADVICE

CHAPTER 9 APPENDICES

Annex 1 Application Form for Special Examination and Approval of Innovative Medical Device
Annex 2 Application Form for Information Communication and Exchange of Innovative Medical Device
Annex 3 Feedback Letter for Application of Information Communication and Exchange of Innovative Medical Device


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