This year gemro will take part in the CPhI / ICSE exhibition for the 5th time. From 2005 – when gemro took part the first time – until today the GMP world in China as well as the related requirements heavily changed. It was the CEP certificate, the ASMF, and DMF documents pharmaceutical manufacturers – mainly API – focused on at the beginning to have a chance to enter the EU and USA market respectively. Over the time it becomes obvious that those documents are closely related to a well established GMP system which should be a western related GMP system much more than a Chinese GMP system. But what are the differences between and what is it what western authorities expect from Chinese manufacturers today? gemro provided several answers on that topic by individual speeches and seminars over the past years. This year again our western experts will be available to provide answers to most critical questions and also you may feel free to ask for a handout of our past seminars. Just come to our booth E1C18 or even arrange an individual meeting with our German consultant Mr. Ralf Gengenbach.

For more information please contact Cobby Zhang; c-zhang@gemro-services.com

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