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FDA Centers FDA Los Angeles District Office And Orange County Regulatory Affairs Discussion Group PresentThe 15th Annual FDAOCRA Educational Conference Sustainable Regulatory Practices at Irvine Marriott June 67, 2012 See These Pages For More Information: Conference Information Page 1 About OCRA Page 2JUNE 6 SESSIONS AM Plenary Sessions Page 3 PM Plenary Sessions Page 4JUNE 7 SESSIONS Breakfast Meeting Page 5 AM Plenary Sessions Page 6BREAKOUTS Devices & IVDs Page 7 Drugs/Biologics/...
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FDA Centers are specific divisions within the U.S. Food and Drug Administration that focus on different areas of public health, such as drugs, biologics, and food safety.
Manufacturers, importers, and certain other stakeholders in the food and drug industry are typically required to file information with the relevant FDA Centers.
To fill out FDA Centers submissions, stakeholders must follow the specific guidelines provided by the respective center, which may involve submitting online forms or using specific formats for documentation.
The purpose of FDA Centers is to regulate and ensure the safety and effectiveness of various products to protect public health.
Information that must be reported typically includes product details, manufacturing processes, safety data, and any adverse events associated with the products.
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