MEDICAL DEVICE
REGULATIONS IN
ASIA-PACIFIC MARKETS

Conference Date: 20-21 Sep 2011
Conference Ref: N9-8011
Fee: £1250 + VAT
Venue: The Rembrandt Hotel, London

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

Three Reasons to Attend

• Hear about Medical Device Regulations and Developments in China, India, Hong Kong and Singapore
• Gain practical guidance on how to comply with the requirements
• Discover product registration and labelling requirements in Asia Pacific markets

BENEFITS IN ATTENDING

Now that the European Medical Device market is well established, the next growth area is Asia-Pacific. China, together with other countries in this region have all implemented, or are in the process of implementing, their own medical device regulations. This seminar will provide a comprehensive overview of the medical device regulations and developments in China together with other newly regulated markets such as India, Hong Kong and Singapore. Practical guidance on how to comply with the requirements and gain access to these growing markets will be given.

Discover how these requirements are being interpreted and applied and how to maximise on this rapidly growing market. Delegates are invited to send their specific questions to Management Forum prior to the event to ensure these are addressed at the seminar. Please send your questions to Andrea.James@Management-Forum.co.uk

WHO SHOULD ATTEND

This seminar will be relevant to personnel from the medical device industry in the following departments: Business Development, Regulatory Affairs, Registration, Quality Assurance, Marketing, Manufacturing, R&D and Technical Affairs, who would like to gain an understanding of the regulations in this region to gain access to these newly regulated markets.

Please contact andrea.james@management-forum.co.ukif you wish to know more about this course.

Click here to register for this important Seminar.