The 27th GHWP Annual Meeting was successfully held in Shanghai, The People's Republic of China, 27th-30th November 2023. Please find the presentation materials below: Download file No.3-1 SaMD Industry Showcase- Asmaa Awad.pdf No.3-2 SaMD Industry Showcase- XU Qiang.pdf No.3-3 SaMD Industry Showcase- DAI Weiwei.pdf No.4 Regulatory Progress of Digital Health in CHINA- YANG Pengfei EN.pdf No.5 Artificial Intelligence Medical Device - Industry- GAO Yaozong.pdf No.6-1 Artificial Intelligence Medical Device -Regulatory- Hala Alhodaib.pdf No.6-2 Artificial Intelligence Medical Device -Regulatory- BAE.pdf No.7 Robotic - Industry Showcase (Medical devices)- LIU Wenbo.pdf No.8 Medical Robotic Industry Development and Best Practice in Supervision- GUO Shuting.pdf No.9 3D Printing Devices - Industry Showcase- LIU Ming.pdf No.11 NGS & Mass Spectroscopy - Industry Showcase- Brad Spring.pdf No.12 Medical Device Sterilisation the need for industrial- Lambert Byron&Miguel Ávila.pdf No.14 Introduction of Innovative Medical Devices Review- JIA JianXiong.pdf No.15 Regulatory pathways for innovative medical- MIYASAKA Tomoyuki.pdf No.16 Regulatory pathways for innovative medical- Seil Park.pdf No.17 Regulatory pathways for innovative medical- Lailing.pdf No.19 Innovative Regulatory Pathway for Innovative- Philip.pdf No.18 Regulatory pathways for innovative medical- Razan.pdf No.21 Utilizaing the Regulatory Sandbox to Facilitate- Nicole Philips.pdf No.22-1 RWE - tools to support innovation- LIU Yinghui.pdf No.22-2 RWE - tools to support innovation- Heather.pdf No.23 Regulatory convergence & reliance- HUANG Yasha.pdf NO.1 Innovative Practices to Promote the Development- Lyu Xucheng.pdf NO.3 Shanghai MPA Capacity Building Experience- XU Lai.pdf NO.5 The roles of standards for innovative medical device- Peter.pdf NO.6 Standardization drives innovation in medical devices- TIAN Yi.pdf NO.7 Sharing Best Practices on Innovative Pathways for Changes- Adelheid Schneider.pdf NO.8-1 Pre-determined Change Control Plan (PCCP)- Brad Spring.pdf NO.8-2 Pre-determined Change Control Plan (PCCP)- April.pdf NO.9 Post-market Vigilance and Adverse Event Monitoring- KUSAKABE.pdf NO.10 Medical Device Adverse Event Terminology- ZHENG Lijia.pdf NO.11 Hybrid Registry and EHR based Active Surveillance-. GAO Pei.pdf NO.13-1 The role of UDI in whole product life cycle management- WANG Xinbing.pdf NO.14 Good Practice of UDI in Clinical Use- YU Donglan.pdf NO.16 eIFU - Requirements and best practise- Sharad.pdf NO.17 Sharing of the Best Practices for elabels- Diana.pdf
