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Event Organizer ComplianceOnline
Contact Name Referral
Contact Number +1-650-620-3915
Contact Email referral@complianceonline.com
Event Category Conference
Event State/City California
Event Country USA
Cost of Attendance $249.00
Event/Registration URL http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=703313?channel=IFSQN
Event State/City California
Event Country USA
Cost of Attendance $249.00
Event/Registration URL http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=703313?channel=IFSQN
Event Description
This webinar will focus on the different types of import alerts issued by the FDA. It will provide the attendees strategic recommendations for removing one’s company and/or products from an import alert.
Why Should You Attend:
An import alert allows the 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 knows 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 the FDA to place a product, manufacturer, shipper, grower, geographical area, and/or country on import alert.
This webinar will provide attendees with background about FDA import alerts, examine why there are issues, where to locate them, how to find out whether a company or product is the subject of an import alert, and finally, provide a series of strategic recommendations for removing a company or product from an alert.
Learning objectives:
- 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.
- Understand 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.
- Know 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.
- 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
This webinar will be beneficial for the individuals in pharmaceutical, biologics, animal health, food, medical device and other biotech companies. Following personnel will benefit:
- Regulatory Affairs
- Managers
- Consultants
- Scientists
- Research Analysts
- State Policy Officials
- Insurers focusing on Representations & Warranties Insurance
- Investment Analysts
- Venture Capitalists
- Labelers
- Product Distributors
- Importers, Customs Brokers
- Financial analysts and investors watching the pharmaceutical, life sciences and biotech industries
Karl Nobert, is a Food and Drug Regulatory Attorney in Washington, DC. Mr. Nobert regularly provides FDA regulatory advice and counseling to domestic and international pharmaceutical, medical device, OTC drug, medical devices and veterinary drug companies. He advises his clients on issues related to the FDA’s regulation of their products and provides them with strategic recommendations for regulatory compliance and mitigating potential enforcement risk. He frequently presents and has published on such topics.
