The Division of Drug Information (DDI) is CDER's focal point for public inquiries. We serve the public by providing information on human drug products and drug product regulation by FDA.
Simply, we listened to you. We evaluated our Web site with a sampling of our key audiences:
- consumers
- health professionals
- industry representatives
Through collaboration with users in testing site-wide designs, we made improvements to make FDA.gov easier and more satisfying to use.
What is different about the new site?
We've created new features that will allow you to find information more quickly. Some examples:
- Information is categorized by topic for easier retrieval, with related subjects consolidated in sections on the site.
- Page design and navigation have been updated and are consistent throughout the site.
- Content has been reviewed for relevance, with redundant and outdated content removed.
This is just the beginning!
The redesign is part of an ongoing evolution that began in 2008. We will continue to evaluate our site regularly and incorporate feedback from our users.
We'd like to hear from you --
Please give us your comments on our new Web site at: http://www.fda.gov/AboutFDA/AboutThisWebsite/AbouttheWebsiteRedesign/default.htm
This is an automated message delivery system. Replying to this message will not reach DDI staff. If you have comments or questions, please contact us at: 1-888-INFO FDA (1-888-463-6332) or (301) 796-3400 from 8:00 am - 4:30 pm Monday - Friday. You can also email us at druginfo@xxxxxxxxxxxx.
For additional drug information, please visit our DDI websites: http://www.fda.gov/cder/Offices/DDI/default.htm and http://www.fda.gov/cder/Offices/DDI/pathfinder.htm.
Update your subscriptions, modify your e-mail address, or stop subscriptions at any time on your Subscriber Preferences Page. You will need to use your e-mail address to log in. If you have questions or problems with the subscription service, please contact support@xxxxxxxxxxxxxxx.
This service is provided to you at no charge by U.S. Food & Drug Administration (FDA).
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