How to Use Foreign Trade Zones and Bonded Warehouses

Duration: 60 Minutes
The use of Foreign Trade Zones and Bonded warehouses for FDA regulated products create different opportunities and different obligations. Firms need to understand the requirements of each to use them to their advantage. The imported products will have different regulatory requirements depending on the option chosen. In some cases, FDA does not give you an option and the outcome is expensive. Firms also must consider the physical security and controls of their products. Theft, loss, damage or diversion must be factored into your decisions. Your choices need to consider the risks posed by using one approach versus another. Your cargo shipment may be very valuable and should be treated as such.
Foreign Trade Zones and Bonded Warehouses
Instructor: Casper E Uldriks
Product ID: 509658
Objectives of the Presentation
  • The role of Foreign Trade Zones (FTZ)
  • The role of Bonded Warehouses
  • The Food and Drug Administration's regulatory role
  • Customs and Border Protection regulatory controls
  • Product security
  • Record keeping
  • Reporting
  • Managing Bulk Active Pharmaceutical Ingredients
  • Pros and Cons of using FTZs and Bonded Warehouses
Why Should you Attend
The webinar covers how use of Foreign Trade Zones and Bonded Warehouses to your advantage and what obligations there are for FDA and the U.S. Customs and Border Protection service (CBP). There are pros cons to using each, and there are different regulatory requirements for CBP and FDA. Some imported products will never have an easy path.

Who will Benefit
  • Initial Importers of FDA regulated products
  • Owner of Record for Entries
  • FDA registered U.S. Agents
  • Import Logistics Managers
  • Foreign Manufacturers
  • U.S. Manufacturers
  • Import-for-export Manufacturers
  • Customs Brokers
$249
Recorded Session for one participant
Get life time access with download option!
Book this course
Pay Now
  $329.00 Training CD
Free shipment within 4 Working Days of placing the order. Get life time access for unlimited participants.
  $379.00 Training USB Flash Drive
Free shipment within 4 Working Days of placing the order. Get life time access for unlimited participants.
For multiple location please contact our customer care team +1-510-857-5896.
How it works
Live Session - How it works
  • Login to onlinecompliancepanel with your registered username and password https://www.onlinecompliancepanel.com/login
  • The webinar joining link, username and password for joining the webinar will be updated on your OCP Account 24 hours prior to the webinar
  • Presentation handouts in Downloadable PDF format will be updated on your OCP Account 24 hours prior to the live session
  • Login to the audio conference on the scheduled date and time
  • Get answers to your queries through interactive Q&A sessions via chat at the end of the session
  • Download the Certificate of Attendance and Purchase Invoice from your OCP Account 24 hours after the completion of the session
  • Please let us know your thoughts and views at the end of the webinar, your valuable feedback will help us improve
Recorded Session - How it works
  • Login to onlinecompliancepanel with your registered username and password https://www.onlinecompliancepanel.com/login
  • Upon purchase of the recorded session a link will be updated on your OCP Account within 24 hours
  • Please click on the link to access the Recorded Session
  • Presentation handouts in downloadable PDF format will be updated on your OCP Account within 24 hours of the purchase of the product
  • Download the Certificate of Attendance and Purchase Invoice from your OCP Account after 48 hours of the product Purchase
  • Please share your valuable Feedback at the end of the session
Instructor Profile:
Mr. Uldriks held a number of positions at FDA, such as an investigator in FDA's New England office, in the Office of the Commissioner in Legislative Affairs and in the Center for Devices and Radiological Health (CDRH), where he served as CDRH's Associate Director for Regulatory Guidance and Government Affairs. He helped to guide CDRH to develop and implement various medical device related amendments to the Food, Drug, and Cosmetic Act, regulations and guidance documents. For years he has trained FDA staff on medical law and has been a featured speaker at many professional conferences involving FDA's medical device program.
Bar Admissions: Massachusetts, 1986 and District of Columbia, 2011
Education: Suffolk University Law School, Boston, Massachusetts, 1986.
View More