Medical UDIs and Traceability Forum
May 16 - 18, 2017 - Brussels UKIQPC UK
enquire@iqpc.co.uk
Phone:+44 (0)207 036 1300
Europe's Dedicated Healthcare UDI Conference is back to ensure that your company is maximising it's efforts for improving compliance, whilst maintaining your competitive edge! Through regulatory discussions, panels, roundtables and practical case studies, this forum is tailored and uniquely positioned to highlight the state of urgency in the industry, address implementation challenges - plus maximise the ROI of your UDI implementation in the future, ensuring it continues to drive business value. As UDI implementation continues in the North American regions, the global medical device industry is beginning to focus upon imminent European regulatory changes and the upcoming implementation for these geographies. Regulatory bodies, device manufacturers, healthcare providers and numerous other stakeholders are gearing up for implementation in region which presents it's own specific challenges and opportunities. Adherence to European specific regulatory specifications, both in labelling and packaging as well as data is a must, but in an increasingly competitive market, achieving compliance whilst maintaining a competitive edge and assuring ROI is of paramount importance also. What if you get audited by the FDA? There has already been at least one FDA 483 warning letter citing UDI non-compliance; what can you do to make sure you're protected?