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Evanston, IL6/8/2015 - 6/11/2015
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An analysis of the impact of FDA’s four expedited programs on
development and review of drugs for serious conditions over the last two-and-a-half
years since breakthrough therapy designation was introduced, including a
Welcome to Regulatory Reconnaissance, your daily regulatory news and intelligence briefing. We're back from a brief vacation hiatus. Today's Regulatory Recon includes all the major stories you might have missed between 23 May and today.
The Nuffield Council on Bioethics has released a report on the ethical issues surrounding clinical research involving children in the UK and EU.
In Geneva Monday, members of the World Health Assembly (WHA) endorsed a plan to fight antimicrobial resistance (AMR) on a global scale.