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The U.S. Food and Drug Administration's (FDA) Center for Devices and Radiological Health (CDRH), Center for Drug Evaluation and Research (CDER), and Center for Biologics Evaluation and Research (CBER) are pleased to invite you to the virtual 2022 Regulatory Education for Industry (REdI) Annual Conference. 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.
When:
- June 6-7: CDER Drugs track
- June 8-9: CDRH Devices track
- June 9-10: CBER Biologics track
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