Strategies to Manage the Complexity of Setting Up Clinical Trials in Emerging Markets – 1

24 October 2018
Available Seats:

The attendee will be able to:

1. Describe three (3) situations where knowledge of regulatory requirements can positively influence clinical supply chain outcomes
2. Summarize how differences in emerging market regualtory requirements can effect shipping and distribution channels
3. Present the best way you can be aware of, and access, changing merging market regulations for clinical supplies used in global clinical trials

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