FDA Transparency Blog

Today, as part of the third phase of the Transparency Initiative, FDA launched a web-based resource called FDA Basics for Industry to provide basic information about the regulatory process, including information that is frequently requested by industry.  

FDA Basics for Industry includes:

• Easier access to frequently requested content, including, guidance documents, information about the review process, and registration and listing information
• Links to training modules for industry, such as the Center for Devices and Radiological Health’s CDRH Learn educational tool
• Answers to questions frequently asked by industry

The launch of FDA Basics for Industry is one of the 19 steps outlined in a report issued today by the Transparency Task Force about ways FDA can improve its transparency to regulated industry.

Visit FDA Basics for Industry and let us know what you think.  You can leave a comment on this blog or send an email to webmail@oc.fda.gov.

Afia Asamoah, Transparency Initiative Coordinator