September 24, 2024, PM | Hotel Conference Room

Background:

In recent years, there has been significant momentum in the development of medical-industrial integration, driven by advancements in science and technology. Simultaneously, the growing demand for medical and healthcare services has created a significant need for domestically produced, independently controllable, and advanced medical-industrial combination products.

In the 1960s and 1970s, many research universities in the United States began focusing on the intersection and integration of medicine with various disciplines and made substantial investments in interdisciplinary medical-industrial research. Currently in China, the government has implemented a series of policies to incentivize enterprises to engage in original innovation. Many local governments have also introduced policies to support clinicians in participating in medical device technology innovation. They are actively promoting collaborative research and development of medical devices and exploring incentive mechanisms for clinical trial organizations and medical staff to drive medical device innovation.

The introduction of the medical device registration system has created new opportunities for the advancement of the medical device industry. On April 3, 2024, the State Drug Administration issued a notice to enhance the oversight and management of the contracted production of medical device registrants, further bolstering the supervision and management of the contracted production process. By safeguarding scientific research accomplishments to foster innovation, it effectively mitigates risks associated with the quality and safety of medical devices.

This conference will concentrate on trending issues and information in the realm of medical-industrial integration, with a special focus on artificial intelligence, biomaterials, and other groundbreaking technologies and materials. Renowned industry experts will be invited to come together and engage in discussions, sharing insights on expediting the development of vital core technologies, facilitating the localization of high-end medical equipment, and implementing the application of research outcomes from medical-industrial integration in clinical settings. Furthermore, they will delve into the future prospects of medical-industrial integration.

Participants:

• Medical device manufacturers: heads of departments and projects/enterprises engaged in medical device R&D, quality, production, etc.
• The enterprises engaged in medical device regulation consulting, research and services.
• Medical device regulatory agencies and research organizations

Agenda:

*The agenda may be subject to changes due to adjustment of confirmed speakers