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Organised By
Speakers:
 
 
Yutao Hua
Yutao Hua
Division Chief, Chemical medicine and medical device division
National Center for Biotechnology Development, Ministry of Science and Technology of PRC
Senyong Lin
Senyong Lin
Deputy Director
Medical Equipment Safety Supervision Department of SFDA
Shaolei Tian
Shaolei Tian
Professor/Deputy Director of 3rd Inspection Division
Center For Certification Of Drug, CFDA
Yanruo Xu
Yanruo Xu
Former Officer
Regulation section of medical device safety, Shanghai Food and Drug Administration
Dr. ChandrasiriJayakody
Dr. ChandrasiriJayakody
Director of Research & Development-Foam Technologies
Filtrona Porous Technologies
Yong Song
Yong Song
Vice President of R&D
Clinical & Regulatory Affairs,Bonovo Orthopedics, Inc
Dr. José Fernández Villaseñor
Dr. José Fernández Villaseñor
Medical Segment Manager and engineering expert
Freescale Semiconductor
Dr. Xiaoyan Gong
Dr. Xiaoyan Gong
President
Medical Implant Mechanics LLC
Florence Chua
Florence Chua
China Director
Regulatory Affairs Professionals Society
Joalin Lim,
Joalin Lim,
VP for Regulatory Affairs
Agape Life System Support
FarajAbdelnour
FarajAbdelnour
President& Director
ACIDIM Association &Synergus AB
Annie Yin
Annie Yin
Regulatory Affairs Director
Medtronic China
Roby Liu
Roby Liu
Investment Director
ZEVC
Dr. Ye Li
Dr. Ye Li
Director
Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences
Meikui Zhang
Meikui Zhang
Director/Associate Chief Physician
Wireless medical center, The general hospital of Chinese People's Liberation Army
Guanhua Ren
Guanhua Ren
Director
China National Institute of Standardization
Dr. Timothy Low
Dr. Timothy Low
Vice President for Medical Affairs
Covidien
Wei Li
Wei Li
Director & Professor
Director for National Center for Fuwai Cardiovascular Diseases China, Visiting Professor for The Chinese University of Hong Kong, Expert Review for Clinical Trials, SFDA
Liang Qian
Liang Qian
BSI APAC MD Regional Lead & Orthopedics Expert
British Standard Association
Dr. Guixin Shi
Dr. Guixin Shi
R&D Director
Beijing Advanced Medical Technologies,Ltd.Inc
Scott Yu
Scott Yu
Independent regulatory consultant
Regulatory VP for Sterilance Medical, Contract Supplier Auditor for J&J, Zimmer and Abbott, Expert for FDA & CE regulation
Chunren Wang
Chunren Wang
Director
National Institutes for Food and Drug Control (NIFDC)
Chuan Yao
Chuan Yao
Vice President/ Senior Consultant
Pacific Bridge Medical (PBM)
Long Yang
Long Yang
Chief Operation Officer
Shenzhen Hlongmed Biotech Co.,Ltd.
 
 
Attendees List
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Background
  • The development scale of medical devices in China is over hundreds billion Yuan, and the annual average growth rate is near 23%. The market scale will be 340 billion Yuan in 2015 by expected. Comparing with 42%, the number that medical devices accounts for the whole medial market in global, the number in China is only 14%. Therefore, there is great space for development in the future for China.
  • Chinese government has large input to medical devices market, from the perspective of policy, there are “Twelfth five-year" science and technology special planning for medical device industry and Health China 2020 Strategy Research Report by ministry of technology and health. And besides, in next eight years Chinese government will launch seven major projects of large health systems, and the investment amount is RMB 400 billion.
  • As for the market trend, the demand for medical devices will increase with the increase of aging population. And there are two major opportunities in this industry, import substitution and upgrade.
  • Challenges and opportunities are obvious in this industry, which are covered in the conference agenda: updates of the regulations in China and overseas and the difficulties in registration; design and innovations of medical devices; the standard and methods of risk assessment and quality control; application of new materials; development of wireless/mobile medicals.

    Under the background above,MDiT Forum and Regulation Summit 2013 will be held on 24th-26th September at Shanghai World Expo Exhibition and Convention Center.
Why Should You Attend?
  • International influence of MEDTEC and brand recognition
  • In-depth networking and communication between medical devices manufacturers and suppliers
  • Exploring the latest regulations and techniques in medical device industry
  • Updating of new topics like design & innovations, wireless/mobile medical devices
  • Rich format on site to give you more opportunities to communicate with experts and decision makers in this industry
Introduction of Medtec:
MEDTEC China 2012, held 26-27 September 2012 in Shanghai, once again proved it was THE event on the Asian medical device manufacturing calendar. Held at the all-new Shanghai World Expo, the total number of 360 exhibitors including co-exhibitors enjoyed the attendance of 7, 239 qualified trade visitors representing a is 6.8% increase in the number attending in 2011.Furthermore, the comprehensive conference program once again proved a popular feature of the show, with both conference rooms (technical forum and regulation) packed to the rafters.
MEDTEC China 2013 will take place on September 25-26 at the same venue as last year, Shanghai World Expo Exhibition & Convention Center, but on an upper level more convenient for all attendees.

Who Should Attend?

Industry Breakdown

 

Job Title Breakdown

 
Doctors/Clinicians
Medical Devices Manufacturers
Machine Tool Suppliers
Materials
Medical Packaging
Medical OEMs
R&D Outsourcing
Health IT Providers
Assessment Agencies
Research Institutes
Others
CEOs and GMs
Heads of
Regulatory affairs & Registration
Research & Development
Technology
Quality
Manufacturing
Supply Chain
Business Development
Strategy
Tendering & Market Access
Others
Media Partners