The Regulatory Education for Industry (REdI) Conference is an FDA-led forum that brings together the regulatory educators from FDA’s Center for Drug Evaluation and Research (CDER) and Center for Devices and Radiological Health (CDRH). The goal of this conference is to provide direct, relevant, and helpful information on the key aspects of drug and device regulations. Our intended audience is the small manufacturers of drug and/or device medical products who want to learn about how FDA approaches the regulation of drugs and devices.

 

 

Because the regulatory principles of drugs and devices are both similar and different, the REdI Conference features several cross-cutting sessions addressing issues common to both drugs and devices, as well as individual break-out sessions which focus on the unique issues of drugs and devices.

 

 

Advance registration is required

Registration is FREE and includes training materials only.

We are going GREEN! Materials will be provided via flash drive upon conference check-in.

WiFi/Internet will be available in the meeting area.

The meeting will NOT be webcast or taped. Flash drives and presentation files will not be available for mailing or emailing. You must be present to receive the materials flash drive.  

 

   

Note: Venue is accessible to persons with disabilities. If you have any special accommodation needs, please make requests as soon as possible to Debbie Levi at debbie@tepgevents.com