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Find Out More About FDA: New Questions and Answers Available on FDA Basics
Based on comments from the public, FDA has added 7 new questions to FDA Basics, the web-based resource that provides information about FDA and what the agency does. Below is a sample of some of the new questions about FDA and the work we do.
How do I report a bad reaction to medicne or medication error to FDA?
Is FDA responsible for regulating pesticides that are used in animal products?
Find out answers to these questions and more at FDA Basics!
Afia Asamoah, Transparency Initiative Coordinator

I had no idea EPA and FDA shared the responsibility of regulating the pesticides as they relate to animal products.
It’s great to see agencies work together; however, I am sure it creates some problems as well. Streamlining such tasks might be a good thing, when applicable.
Respectfully,
Ana Hoffman
Many people are trying to find some answers about FDA. It is good to read that FDA really cares constantly expand information about their work. Recognition and detailed answering of question will certainly contribute about positive influence to us, just an ordinary people who usually don’t know much about FDA.
Are there any PowerPoint presentations about FDA, its work and FDA basics? Where to find them?
It would be great if you have them on slideshare.net or anywhere else available for everyone.
I second Ana, and thanks for the info about reporting by consumers in MedWatch program. As a paralegal I can now tell clients to fill the form by themselves.
In my opinion, FDA is a very important organisation. Crucial for its acceptance is an honest information policy so that people know and understand what FDA stands for. Many young people have to be taken care of and FDA should to try to reach those people who really need advice.
You can find PowerPoint presentations from FDA Basics webinars at http://www.fda.gov/fdabasics. Click on “Ask Us: FDA Basics Webinar Series.”
After reading your post, I thought your thoughts were very naive but as I kept reading on, I do see you have a point. Keep on writing, I will keep on coming by to read your new content.
I second Ana, and thanks for the info about reporting by consumers in MedWatch program. As a paralegal I can now tell clients to fill the form by themselves.
G’Day! Fdatransparencyblog,
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Cheerio
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