is being presented by Jeremy Yung, Regulatory Affairs Associate, with ArthroCare Asia Pacific and airs on Wednesday, May 11th, 2011. For more details, or to register please visit our site at www.fxconferences.com
The regulatory environment for medical devices in Asia Pacific has changed significantly in the last five years. Countries that had little or no regulation have now implemented full pe-market reviews, quality systems control and post-market enforcement.
This audio conference presentation provides a country-by-country overview of the changes that have taken place in recent years, and what device companies can expect moving forward. Our speaker discusses the primary Asian markets, and the steps being taken by countries in this region to harmonize and increase the efficiency of device registration. The presentation reviews these developments in detail, and weighs in on how this new landscape will affect life sciences companies in the future.
