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26 days to go - register NOW!
Medical Device and IVD Regulations in Asia Pacific
19 - 21 June 2012, Estrel Hotel, Berlin, Germany
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Medical Device and IVD Regulations in Asia-Pacific
Update on regulation for medical devices and IVD across 13 Asia-Pacific countries
Informa Life Sciences' annual Medical Device and IVD Regulations in Asia-Pacific conference is back for its sixth year!
Don't miss this opportunity to get critical updates on regulation from key Notified Bodies with 6 representatives from Underwriters Laboratories, SGS, TUV SUD and BSI Healthcare plus strategic insights from senior level industry representatives for successful registration strategies and market access in Asia-Pacific.
2012 Conference Highlights: Latest updates on regulation and market access across China, Japan, India, Saudi Arabia, Australia, New Zealand, Taiwan, Hong Kong, Korea and key ASEAN markets
- Critical update on the changing regulatory landscape and successful market access in China read more
- Examining the latest regulatory updates in Japan read more
- Understanding the current regulatory environment in India and Saudi Arabia read more
- A regulatory update from Australia and New Zealand read more
- An overview of the regulatory system in Taiwan and Hong Kong read more
- Exploring medical device & IVD regulations in Korea read more
- Review of Key ASEAN Markets: Malaysia, Indonesia, Singapore, Thailand read more
Asia-Pacific Expert Speaker Panel
Asia-Pacific Expert Speaker Panel
Jack Wong
Director Regulatory Affairs
Johnson & Johnson
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Saleh Al Tayyar
Vice Executive President for Medical Devices Sector
SFDA
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Ed Woo
Regulatory Affairs Director
Medtronic Inc, USA
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Renee Hardley
Regulatory Affairs Manager - Asia Pacific
Cochlear Limited, Australia
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Media Partners
Asia-Pacific Evening Seminars
EVENING SEMINAR X: Tuesday 19 June 2012
Essentials of Establishing Clinical Programs in China for Medical Device Studies
EVENING SEMINAR Y: Wednesday 20 June 2012
Success in Key Latin American Markets: Regulatory Updates and Effective Market Access
Who Should Attend?
Heads of Department, Directors, Managers, Team Leaders, Associates, Specialists and Coordinators from:
- Regulatory Affairs
- Regulatory Affairs - Asia-Pacific
- Quality Assurance
- International Regulatory Affairs
- International Health Policy
- Global Regulatory Operations
- Global Registration
- Worldwide Quality Control
- Regulatory Documentation
- Business Development
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Dates and Venues
19 Jun 2012 - 21 Jun 2012
Estrel Hotel, Berlin, Germany
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Reviews
"A most enjoyable and informative conference"
"Good networking with a high value of content"
"Informative, challenging, entertaining! The most useful event I have ever attended – broad coverage, detailed information of practical advice. Excellent networking opportunity!"
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