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26 27 28 29 30 * CRO / VENDOR MANAGEMENT IN THE PHARMACEUTICAL INDUSTRY
 31 * THE NEW ROLE OF THE QUALIFIED PERSON UNDER THE MEDICAL DEVICES DIRECTIVES
  
MEDICAL DEVICES
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MEDICAL DEVICE
REGULATIONS IN THE
ASIA-PACIFIC MARKETS

Gain practical advice on how regulations are being
applied to enable you to maximise on this rapidly
growing market

Conference Date: 11-12 Dec 2012
Conference Ref: N12-8112
Fee: £1255 + VAT
Venue: Harrington Hall Hotel, London

BENEFITS IN ATTENDING:

  • Gain an understanding of medical device markets in Asia
  • Hear an update on the Asia Harmonization Working Party (AHWP) and ASEAN
  • Take away practical experience of hos to license a medical device in China
  • Comply with the requirements of the Japanese Ministerial Ordinance 169
  • Discover the product registration requirements in India
  • Gain an insight as to future developments in Hong Kong, Singapore, Malaysia and Taiwan
  • Receive key advice on gaining access to these markets

If you have any queries please click here to email Andrea James

 

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