Due to unforeseen circumstances, we regret to announce Global Medical Device Packaging and Labelling Compliance will not take place as planned on the 24th to the 26th of January. We would like to thank you, our speakers and all those involved in supporting the event.

If you have any questions, we’d be happy to answer them – please contact us on:

Freephone: 0800 652 2363 or +44 (0)20 7368 9300
Email: enquire@iqpc.co.uk
Please see the following related events www.pharma-iq.com/events.cfm

18+ Industry Representatives Share their Latest Insights:

Achieving Compliant, Cost Effective and UDI Traceable Packaging and Labelling to Stay a Step Ahead of the Competition

In a landscape of ever increasing and ever evolving regulatory requirements, developing compliant medical devices packaging and labelling is often challenging. Furthermore, the introduction of unique device identification (UDI) by the FDA and in Europe has added complexity to the already multifaceted medical device labelling strategies. In light of this, Global Medical Device Packaging and Labelling Compliance 2011 will provide the very latest practical insights to enable you to achieve compliant, cost effective and UDI traceable medical device packaging and labelling.

Medical Device Industry and Regulatory professionals will share their expertise to help you:

Prepare for the future and capitalise on regulatory change to stay ahead of the market with comprehensive guidance to UDI implementation, which traceable solution to use, practicalities and timelines from B.Braun, BSI and GS1

Develop a globally applicable labelling strategy to boost economic efficiency with practical and regulatory insights from Johnson and Johnson and BSI Group and an interactive panel discussion with industry thought leaders

Develop an effective global symbol use approach compliant with ISO standards to optimise your labelling pipeline and increase productivity with valuable insights into ISO standards from Medtronic, NEN and Coloplast

Benchmark against competitors with critical insights into the evolving regulatory requirements and medical device directive to achieve complete alignment in your global labelling strategy; updates from medical device companies including Bard and Toshiba Medical Systems

Advance your labelling systems through integration of e-lablleing at minimum economic impact with strategies from Medtronic, Radiometer and GE Healthcare

Achieve transparency over your supply chain through understanding of AIDC and EU requirements in hospitals to maximise patient safety and reduce the frequency and cost of adverse events with GS1 Germany and the Department of Health

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