How to Register Medical Devices in China 101 | Cisema Webinar

Learn the fundamentals of medical device registration in China with a clear, step-by-step overview of NMPA (National Medical Products Administration) requirements. This webinar explains how classification, testing, and clinical pathways work in practice, helping regulatory and market access teams prepare for a successful China entry. Professionals entering or expanding in the Chinese medical device market will benefit from concise guidance, practical strategies, and real case examples from Cisema’s specialists. For more information, explore our medical device registration in China services: https://shorturl.at/Cp8RQ Webinar Speakers: Hamish King – CEO, Cisema (  / hamish-king-328667191  ) Jacky Li – Hong Kong RA Lead, Cisema (  / jacky-li-9791b8a9  ) Connect with Us: 🌐: https://cisema.com   / cisema   https://x.com/CisemaHK/ ✉️Newsletter: https://us20.list-manage.com/survey?u... About Cisema: Founded in 2002, Cisema is a leading provider of regulatory affairs, quality compliance, clinical research, and product testing and safety certification services across China and the broader APAC region, supporting start-ups to multinationals with product approvals of all classes and specifications. With more than ten global offices and service centers throughout China and Southeast Asia, we enable compliance for medical devices, IVDs, pharmaceuticals, veterinary products, pet food, cosmetics, health supplements, automotive, and toy manufacturing.