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Get ground-breaking regulatory insights, hear renowned experts from across the globe, and partcipate in invaluable formal and informal networking events at the 2008 RAPS Annual Conference & Exhibition. Register today.
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As the global regulatory profession has grown, so has interest in a general, global Regulatory Affairs Certification (RAC). Help RAPS develop this certification by participating in a survey.
Health & Regulatory News
New PhRMA Marketing Code Means No More Free Pens
The Pharmaceutical Research and Manufacturers of America released new voluntary guidelines last week calling for drugmakers to stop the use of free pens and other so-called “reminder” promotional items.   More »		 FDA Changes Format of Nonapproval Letters
When the US Food and Drug Administration notifies companies whose pharmaceutical products are not approved for sale in the US, it will now use a more neutral format called a “complete response letter.”   More »
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Regulatory FOCUS

July 2008: GXPs
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Interested in contributing to Regulatory Focus?

If you would like to submit an article for publication in Regulatory Focus, review the editorial calendars for 2008 and 2009 and pick your issue. The Author Guideline provides answers to most questions about format and submission types (features, departments, letters to the editor). If you need any additional information or have any questions, send an email to editor@raps.org.
Bookstore

New In the Bookstore!
Fundamentals of EU Regulatory Affairs, Fourth Edition is now available to order. This highly acclaimed publication has been updated with expanded facts, regulations and statistics along with 3 new chapters.

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