EU Medical device regulation: philosophy, content and structure Directive 93/42/EC, as amended by 2007/47/EC CE mark ISO 14155, ISO 13485 and ISO 14791 Risk-classification of medical devices Drug-device combination products Clinical evaluation and clinical investigation Medical devices vigilance system Recent and upcoming legal changes in Europe
Who should Attend
Regulatory bodies who would like to get acquainted quickly with all aspects of medical device regulation
Professionals starting work in industry
Professionals in pharmaceuticals
Past Events
Medical Devices: Regulation and Lifecycle Management 2015 - 21-23 Sep 2015, Flemings Hotel Wien - Stadthalle, Vienna, Austria (52891)
Important
Please, check "Medical Devices: Regulation and Lifecycle Management" official website for possible changes, before making any traveling arrangements
