Medtec China 2016 onsite: MDiT Forum and Regulation Summit 2016
Quality Track B: Supply Chain Management and UDI
Afternoon of Oct 27 | Conference Room 16
Supporters: MDTA & CCBMT
As EU and US has launched UDI requirements and principles from 2013, they had conducted UDI from high-risk implantable devices, which provided experience reference for us. Meanwhile, combining the condition of Chinese manufacturers and demand from hospital, UDI is necessary for Chinese medical device industry.
Former RAPS China Chairman, and President from Shanghai Pudong Medical Device Trade Association (MDTA), Mr. Liang YAN devoted to promote UDI practice in China for more than 10 years. Co-organized by Medtec, MDTA and CCBMT, this conference will discuss UDI implementation and supply chain management, to improve the medical device industry development and supply chain efficiency and to ensure the patient safety.
>Apply QMS conception to UDI implementation
>The influence of UDI on GSP, medical informatization and the third-part logistics
>Implementation updates of UDI in US
>Necessary analysis of UDI implementation in China combining with Chinese medical device supervision system
>Q&A for Chinese & US UDI policy and implementation
Who should Attend?
>RA, QA&QC, R&D Department, Project Manager/Director and Managing Director from import/export medical device manufacturers
>Distributors, Third-Part Logistics and Medical informatization suppliers
>Hospitals, surveillance organization and quality & operation control organization
Conference Room of Shanghai World Expo Exhibition & Convention Center
North Entrance, No. 850 Bocheng Rd. Shanghai
Speech & Cooperation
+86-21 6157 3933
Sponsor & Paid Conference
+86-21 6157 3922
Media & Free Conference