Clinical Trials Supply Chain 2013

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Regulatory support is a critical aspect of clinical trial supply distribution, requiring the creation and control of essential documents and activities to ensure a seamless supply of clinical materials. Therefore our two-day event will devote three workshop sessions to the impact of EU guidelines on clinical supplies (GDP/GMP/GCP). Attendees will also learn how to maximize the efficiency and ensure the safety of clinical supplies, gain insight into packaging & labelling solutions, temperature-controlled distribution and much more!
Organizer: Fleming Europe

20 Nov 2013

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