The Food and Drug Administration's (FDA's) Center for Drug Evaluation and Research (CDER) and Center for Devices and Radiological Health (CDRH) are pleased to announce a co-sponsored seminar developed just for you:
FDA Small Business Regulatory Education for Industry (REdI) Conference
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.
WHEN: June 19 – 20, 2012
WHERE: The Westin O'Hare
6100 North River Road
Rosemont, IL 60018
Advance registration is required.
Registration is FREE and includes training materials only.
We are going GREEN! Presentations will be made available via flash drive upon sign in.
The meeting will NOT be webcast or taped.
*The attendee is responsible for accommodations, meals and hotel parking.
To Register, click here.