The regulatory landscape and fast approaching FMD deadlines have continued to drive the industry forward over the last 12 months.

But even with these significant strides, it is clear that there is a vast difference in terms of the stages each organisation is at, and how they are tracking to meet the deadlines.  Some organisations are well ahead, with testing and deployment underway; whilst others are still at the beginning of their journey.

For the organisations  at the beginning, it is critical that the regulatory landscape is well understood, as well as ensuring best practice  project planning, resourcing, supply chain, testing and implementation.

But beyond compliance, many organisations are recognising that serialisation has the ability to transform existing business processes and optimise operational efficiency, and subsequently shifting focus to leverage this area.

If you want to hear more about how serialisation can vastly improve your business, don't miss the Pharmaceutical Serialisation & Traceability Summit 2017!

Across three days, learn about the differences between serialisation regulations globally, how to capture data, format and share it, comply with fast-approaching traceability deadlines, ensure maximum patient safety, manage IT, how to monetize your investment, optimise  supply chain visibility and more.

2017 Speakers Include:

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Implement, Integrate & Optimise Your Sustainable Serialisation Strategy









Pharma Serialisation & Traceability Highlights.

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