Clinical Trials Supply Chain 2013
Organization: Fleming Europe
Venue: Eurostars Berlin
|Event Date/Time: Nov 20, 2013||End Date/Time: Nov 21, 2013|
The key challenge clinical trial supply chain managers face in global distribution is ensuring that supplies arrive at the trial sites on time and in good condition.
Regulatory support is a critical aspect of clinical trial supply distribution, requiring the creation and control of essential documents, study initiation, and activities to ensure a seamless supply of clinical materials. Another regulatory role is labeling management, ensuring adherence to the labeling requirements of different countries, and managing its translation.
MAXIMIZING THE EFFICIENCY of the clinical supplies Ensuring Clinical Supply Chain SECURITY Clinical Supplies in EMERGING MARKETS Overcoming REGULATORY CHALLENGES Temperature-Controlled DISTRIBUTION REVERSE Supply Chain PACKAGING & LABELING Solutions