FDA’s Import Alerts Webinar: Understand the nature of Import Alerts: What are they? What purpose do they serve? What do they mean for a company? – ResearchAndMarkets.com

DUBLIN–(BUSINESS WIRE)–The “FDA’s Import Alerts” webinar has been added to ResearchAndMarkets.com’s offering.

This webinar will provide attendees with background about FDA Import Alerts, examine why they are issues, where to locate them, how to find whether a company or product is the subject of an Import Alert, and finally, provide a series of strategic recommendations for getting off of an Alert.

An Import Alert allows FDA to detain, without physical examination, products that either have or potentially could violate the Food, Drug, and Cosmetic Act (“FDC Act”).

Import Alerts lets FDA Field Staff know that the agency has enough evidence or other information to refuse admission of future shipments of an imported article. There are a variety of factors that could lead FDA to place a product, manufacturer, shipper, grower, geographical area, and/or country on Import Alert.

Once a shipment is refused admission to the U.S., the importer has an opportunity to introduce evidence, within 10 days, to overcome the appearance of a violation. During this time, the product is either held at a warehouse or at the importer’s premises and cannot be distributed. If the shipment is not proven to be safe, it must be destroyed or exported within 90 days.

The alert can be issued for an import from a manufacturer, shipper, grower, geographical area, or country. If the problem or condition exists on a wide scale, federal inspectors would be instructed to detain all products of a certain kind coming from that country.

An imported product, firm, region, or country may remain in this status until evidence or other information is provided that gives FDA confidence that the shipment is safe for consumers and that future shipments will be in compliance with the law. The conditions that the importer has to meet vary depending on the stipulations in the Import Alert.

Learning Objective

• Understand the nature of Import Alerts: What are they? What purpose do they serve? What do they mean for a company?
• Become familiar with CBP and FDA’s shared jurisdiction at U.S. ports.
• Company or Products to be added to an Import Alert.
• Be able to find and search FDA’s Database of Import Alerts.
• Understand the potential and real impact of being named on an FDA Import Alert.
• Be able to identify the steps for removing a Company or Product from an Import Alert.
• What to do if you learn that your products are being detained by FDA at a port and your Company’s name is added to an Import Alert.

Webinar Takeaway

• Import Alerts
• The different types of Import Alert issued by FDA
• What Causes a Country, Company or Products to be added to an Import Alert
• What impact does being named on an Import Alert have on a Company
• What to do if your products are Held or Detained at the port by FDA.
• What to do if your Company or Products are named on an Import Alert.
• Strategic Recommendations for removing one’s Company and/or Products from an Import Alert.

Who Should Attend:

• Regulatory Affairs Professionals, Managers, Consultants, Scientists, Research Analysts, State Policy Officials, Insurers focusing on Representations & Warranties Insurance; Investment Analysts; Venture Capitalists.
• Pharmaceutical, Biologics, Animal Health, Food, Medical Device and other Biotech Companies
• Domestic and Foreign Corporations, Small Business, Start-Up Ventures, Manufacturers, Importers, Labelers and Product Distributors
• Importers, Customs Brokers, Distributors
• Financial analysts and investors watching the pharmaceutical, life sciences and biotech industries

For more information about this webinar visit https://www.researchandmarkets.com/r/xjuboj

Contacts

ResearchAndMarkets.com

Laura Wood, Senior Press Manager

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