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This popular webcast series serves as a study tool for individuals preparing for the RAC (US) Exam.
Online7/15/2015 - 8/19/2015
Online7/22/2015 - 7/29/2015
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Over the past two decades, the US Food and Drug Administration’s (FDA’s) Center for Drug and Evaluation and Research (CDER) has been developing new, expedited pathways to help bring innovative medical products to market more efficiently. These pathways include fast track designation, accelerated approval, priority review and, more recently, breakthrough therapy. Through these expedited pathways, some products have been approved with fewer clinical data than traditionally are required.
A coalition of health advocacy groups are worried that too much of the European Medicines Agency's (EMA) funding comes from private industry.
Welcome to Regulatory Reconnaissance, your daily regulatory news and intelligence briefing.
Since 2007, the US Food and Drug Administration (FDA) has issued a small handful of special "priority review" vouchers which allow its recipient to expedite the review of any one of its new drug products. What are these vouchers, why is FDA issuing them and what benefit might they have for society? Find out in our latest Regulatory Explainer on the Priority Review Voucher system.
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