FDA Regulatory Education for Industry (REdI) - Learning about FDA and Regulatory Science

FDA had their annual conference “FDA Regulatory Education for Industry (REdI)” last week. The REdI conference features three medical product center tracks: Drugs (CDER), Devices (CDRH), and Biologics (CBER). 

The recorded presentations by different tracks (drug, device, biological,...) are available on FDA's website and the conference agenda for this 5-day event is listed here. 

REdI presentations provide opportunities to learn directly from the FDA’s regulatory experts in medical product centers: drugs, devices, and biologics. This course is designed to provide participants with a strong, basic foundation in the FDA’s regulatory requirements.

The recording of the REdI conference are also posted on Youtube and separated by days 1 - 5.

Day 1: 

     

Day 2:

Day 3:

Day 4: 

Day 5: 

In Day 1 presentation by Dr. Bugin, the reorganized structure for various divisions under the Office of New Drug (OND) is revealed.