Keeping abreast of the worldwide regulatory changes in medical device would help related manufacturers reduce the quality risks of packaging and sterilization systems, fulfilling the safety, environmental responsibilities and sustainable development of medical sterilization and packaging industries.
CHINAPLAS together with China Association for Medical Devices Industry Medical Devices Packaging Committee, will hold the International Medical Packaging and Sterilization Forum. Associations, industry experts and relevant leaders of the National Medical Products Administration will share the details of the latest industry standards, regulations and technological developments.
4.18
13:30-17:00
Meeting Room CC204B, Hall 18 (Level 2)
Mandarin
4.18
13:30-17:00
Meeting Room CC204B, Hall 18 (Level 2)
Mandarin
| 13:30-14:15 | Global Regulations on Sustainable Development for Medical Device Packaging | Selena Qin, China Regulatory & Standard Manager of DuPont Healthcare Packaging / Secretary General of China Association for Medical Devices Industry Medical Devices Packaging Committee |
| 14:15-15:00 | End-to-End Microbiological Quality and Sterility Assurance | Sophie Liu, Director ASPAC MD, Microbiological Quality & Sterility Assurance of Johnson & Johnson |
| 15:00-15:40 | Applications of Medical Packaging and Materials | Nina Huang, Marketing Regulation Manager of Shanghai Jianzhong Medical Packaging Co., Ltd. |
| 15:40-16:20 | EO Sterilization Process Validation and Auditing | Li Ning, Senior Director of Quality & Regulatory Affairs of Micro-Tech (Nanjing) Co., Ltd. / Vice-Secretary General of China Association for Medical Devices Industry Medical Devices Packaging Committee |
| 16:20-17:00 | Green and Sustainable Development of Amcor Healthcare Packaging | Li Quanbu, Senior R&D Manager of Amcor Healthcare Packaging |
* The above agenda is subject to change without prior notice, please refer to the onsite announcement.
Cooperating Organization
