As a regulatory professional, confidence comes from having the answers you need. But what do you do when the answers just aren't there? 2014 RAPS will give you the know-how to tackle your toughest issues.
10/1/2014 - 11/30/2014
Improve how effectively you network and advocate for yourself with ideas and techniques from this on-demand webcast.
Local or global—RAPS has you covered with offices in Washington, DC, Shanghai and Singapore. There are RAPS chapters in Canada, Israel, Switzerland, Taiwan and throughout the United States, and local networks in Australia, Belgium, Brazil, Germany, India, Mexico, The Netherlands, Poland and Singapore.
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Among the sessions at 2014 RAPS: The Regulatory Convergence are some that stand out to me, your Regulatory Focus editor, as particularly exciting—sessions that cover important topics, emerging trends, new developments and the critical aspects of actually being a regulatory professional.
Australia’s Therapeutic Goods Administration (TGA) this week (15 September 2014) issued an amended guidance on nonclinical studies for Module 4 of the Common Technical Document (CTD), which is an integral part of an application to register a prescription medicine on the Australian Register of Therapeutic Goods (ARTG).
Welcome to RegBits, a new way to get an at-a-glance look at important regulatory news stories. Today's top stories include the European Parliament taking a hard look at drug pricing, recommendations to improve FDA's 510(k) process, a new chocolate-flavored cough syrup which might cause problems, and two new device reclassifications.
Welcome to Regulatory Reconnaissance, your daily regulatory news and intelligence briefing.