Responsibility 2012.09.11

 

Responsibility 2012.09.11

 

l  Provide training and education in regulatory affairs for professionals working at SFDA and working in the fields of food, pharmaceuticals, medical devices, vaccine, herbal medicine, supplemental dietary and cosmetics in China. Plan, organize, implement, supervise all aspects of the work and guide training work at provincial and lower levels of FDA.

l  Introduce regulatory guidance from EU and FDA, for example, variety of ICH documents, GMP, GLP, GCP, etc.

   

 

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