MEDICAL DEVICE
REGULATION IN ASIA

MEDICAL DEVICE REGULATION IN ASIA

MEDICAL DEVICE
REGULATION IN ASIA

10% DISCOUNT OFFERED TO BSI HONG KONG REGULATORY
FORUM PARTICIPANTS, PLEASE QUOTE HKRF WHEN BOOKING

10% DISCOUNT OFFERED TO BSI HONG KONG REGULATORY FORUM PARTICIPANTS, PLEASE QUOTE HKRF WHEN BOOKING

10% DISCOUNT OFFERED TO BSI HONG KONG REGULATORY
FORUM PARTICIPANTS, PLEASE QUOTE HKRF WHEN BOOKING

MEDICAL DEVICES

Conference Date: 16-17 Oct 2008
Conference Ref: N10-8508
Fee: £1150 + VAT
Venue: The Rembrandt Hotel, London

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.

24 * PHARMACOVIGILANCE ASPECTS OF LICENSING AGREEMENTS
* MULTI-TASKING AND MANAGING MANAGERS

25 * A REGULATORY UPDATE ON ANIMAL FEED ADDITIVES

26 * MANAGING EU FEED ADDITIVE PROJECTS ~ FROM CRADLE TO CRADLE
* BIOSAFETY TESTING

27 * THE EU PHARMACEUTICAL DOSSIER
* OBTAINING AND ENFORCING PATENT RIGHTS IN ASIAN COUNTRIES
* THE TRADEMARK ADMINISTRATOR
* VETERINARY STATISTICS

28 * THE PATENT ADMINISTRATOR