Welcome to the FDAzilla blog! Everything we post here will address this: How can we work smarter with the FDA? While our field is small, it is important, complicated, and sometimes downright odd. We can learn a lot from our collective experiences. In this blog, we’ll share stories from the front lines, perspectives on trends, interpretations of data, and synthesis of industry news you can use. Please check in about once a week, sign up for our blog feed on the sidebar, and follow us on twitter.
Also, feel free to share your comments on the blog, and let me know if you’d be interested in writing a post for us.
A little bit about FDAzilla: We offer data-driven intelligence tools on the FDA for regulatory, quality, and biz dev professionals. One of those tools is our website where we have taken some key FDA databases and made them more usable and searchable – the FDA employee database, MAUDE, 510ks, Devices, Drugs, and 483s.
What tools and information from the FDA would you like to see us build? What information about the FDA would be most useful for you?You tell us, and we may include it in our next round of improvements – we want to build something that’s useful and time-saving for you and your team.
Feel free to contact me with any questions or ideas. You can always reach me at tony@fdazilla.com.
Learn more about how FDAzilla can help you achieve your quality and inspection preparation goals: get 483s, Inspector Profiles, Enforcement Analytics, and GMP Regulatory Intelligence.
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We can show you insights into any of your key suppliers, FDA investigators, inspection trends, and much more.