2013 Regulatory Review and Outlook for 2014

Wim Cypers, Vice President, Regulatory Affairs will review the eventful year of 2013 as it comes to close for Regulatory Affairs professionals. He will assess the situation as it stands for xEVMPD initiative of the EMA, the IDMP initiatives at FDA, EMA and other regulatory authorities as well as the FDA’s UDI initiative for Medical Devices industry regulation.

Then Wim will try to peek a little into the near future to present an outlook of what 2014 may bring in terms of fresh regulatory initiatives and development of initiatives under progress.


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