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CPhI Panel to Analyse New Industry Perspectives and Innovations Ahead of Predictive 2014 Annual Report
Date:7/16/2014

dominantly focussed on the Indian market, Dilip Shah also returns covering the intellectual property rules around innovation. Brian Carlin, who chairs IPEC Americas Excipient Qbd Committee, is also returning. He serves as the director of Open innovation at FMC and received the IPEC One World Regulatory Excellence Award in 2014. The winner of several FDA Commissioner Awards, Dr. Ali Afnan is another well-respected industry influencer and was a key contributor to the drafting and finalising of the current FDA Process Validation Guidance.

Emil Ciurczak, previously a member of the FDA's PAT committee and president of Doramaxx Consulting draws upon his expertise across PAT, QbD and spectroscopy. Finally, William Botha, a respected trainer and mentor in manufacturing is also retuning to the panel; he is fluent in FDA regulations, including GDP and GMP.

Last year's report examined major issues and developments across the industry including regulatory challenges from a globalised industry, cost savings through QbD and PAT, to the effect breakthrough drugs like ADCs will have on overcoming future disease pathologies.

"The 2013 report was hugely successful with our experts providing insights into how the industry will adapt in the near future. This year we have been able to see the progress the industry has made along with the new challenges and threats ahead. Our experts will examine future potential breakthrough drugs, regulatory risks and supply chain issues. This year we also have representation from leading global CDMO players, Patheon, Almac and Arevipharma- adding a further depth of perspectives and providing a completely holistic picture of the
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