Biostatistics in development of Medical Devices By T. Mudde - Clinquest (Qserve Conference 2013) Clinical Impact of the New EU Legislation on Medical Devices By D. Giroud - WMDO (Qserve Conference 2013) New EU Legislation on Medical Devices By G. Bos - BSI (Qserve Conference 2013) Software and Smartphone Applications By E. Vollebregt - Axon Lawers (Qserve Conference 2013) Validation of sterile Medical Devices manufacturing processes By J. Havel - Havel tuv sud (Qserve Conference 2013) Unannounced factory inspections by Notified Body By D. Ziel - Med cert (Qserve Conference 2013) Latest update Korean Regulations By Y. Kim - Synex (Qserve conference 2013) Latest update China Regulations By S. Huang - Qserve Group (Qserve conference 2013) Latest update USA Regulations By P.Trisler Qserve Group (Qserve Conference 2013) Latest update Brazil Regulations By S. Jaime - Qserve Group (Qserve Conference 2013) Potential effects of the upcoming Regulations By Dr. J O’ Dwyer -NSAI (Qserve conference 2013) Post Market Clinical Surveillance, Experience of the Industry by S. Menzl - Abbott Medical Optics (Qserve Conference 2013) Clinical evaluations and impact of the new Regulations y R. Higgins MHRA ( Qserve Conference 2013) Opening Qserve conference 2013 - W. Driessen 
