聚焦器械创新 赋能产业发展——创新医疗器械申报专题培训在苏州成功举办

Group 1 - The training session aimed to enhance the quality and efficiency of innovative medical device application submissions, aligning with the State Council's directive for high-quality development in the pharmaceutical industry [1][3] - Over 10,000 participants from regulatory bodies, production companies, research institutions, and medical organizations attended the training, indicating strong interest and engagement in the topic [1][3] - Experts from the National Medical Products Administration provided insights on key aspects of the innovative medical device review process, addressing common issues and emphasizing the importance of clinical evaluation [3] Group 2 - The training focused on practical guidance for applicants, helping them navigate the innovative review application process and improve their understanding of clinical trial design and objectives [3] - The event fostered a collaborative environment where participants discussed common challenges and solutions, reinforcing a shared vision for the development of innovative medical devices [3] - This initiative serves as a significant step towards implementing national reforms in pharmaceutical regulation and enhancing the research and compliance capabilities of the medical device industry [3]