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.

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 semina