2-day In-person Seminar on “FDA's and the U.S. Customs Border Patrol's Import and Export Control Program” in Los Angeles, CA
August 21 - 22, 2014 - Los Angeles CA USGlobalCompliancePanel
support@globalcompliancepanel.com
Phone:800-447-9407
Fax:302-288-6884
Overview: FDA's and the Customs and Border Patrol Service (CBP) has become increasingly sophisticated and equally demanding in the submission of information and adherence to government procedures. Firm's that fail to understand and properly execute an import and export program find that their shipment is delayed, detained or refused. A number of factors can derail the expectation of a seamless import process. The course covers detailed information about the roles and responsibilities of the various parties involved with an import operation and how to correct the weakest link(s) in the commercial chain. The course will include tips on how to understand FDA's thinking and offer anecdotal examples of FDA's import program curiosities. Why should you attend? What happens when your product is detained? FDA will begin a legal process that can become an expensive business debacle. You must respond fully within short timeframes. This is not the time for you to be on a learning curve. You need to have a plan in place and know what you are doing. The FDA is steadily increasing the legal and prior notice information requirements. If you do not know what those requirements are and you initiate a shipment, your product is figuratively dead in the water. You must be accurate with the import coding information and understand the automated and human review process. If not, you can expect detained shipments. What happens when FDA decides you should bring the products back to the port of entry after you received a release but you cannot locate the product that has been sold? CBP may fine you three times the value of the shipment. FDA may have other adverse legal concerns and strategies. When products are refused, you have different options. Some options may cost more than others. For example, your product may be destroyed by the government. You may be fined if you do not act in a timely manner. These are common problems that become prohibitively expensive. You should know how to avoid common problems or at least how to mitigate the cost by using established and effective business planning. Who Will Benefit: 1. Domestic importers 2. Foreign exporter 3. Initial importers 4. International trade executives 5. Venture Capitalists 6. Marine insurance underwriters 7. Import Brokers 8. Regulatory affairs managers 9. Import / Export consultants 10. In-house counsel 11. Contract specialists 12. Logistics managers 13. Third party establishment inspection entities 14. Sales managers 15. Investors Course Outline/Agenda: Day One Lecture 1: FDA Import History and Legal Authority Customs and Border Control (CBP) Import Process FDA Import Process Lecture 2: FDA Import Process (continued) • Import Brokers • Prior Notice Information Lecture 3: FDA Import Process (continued) • Import Brokers • Bonds and Bonded Warehouses • FDA "Notice of Action" Lecture 4: Import Detention Import Delays Import Alerts Day Two Lecture 5: Foreign Inspections FDA 483 Inspectional Observations Lecture 6: FDA Warning Letters Lecture 7: Import Hypothetical FDA Import for Export Program FDA Export Program Export Hypothetical Lecture 8: FDA Export Program ( 5 Minute Break ) Special Import Issues Instructor/ Speaker Profile: Casper (Cap) Uldriks brings over 32 years of experience from the FDA. He specialized in the FDA's medical device program as a field investigator, served as a senior manager in the Office of Compliance and as an Associate Centre Director for the Centre for Devices and Radiological Health. He developed enforcement actions and participated in the implementation of new statutory requirements. He is recognized as an exceptional and energetic speaker. His comments are candid, straight forward and of practical value. He understands how FDA thinks, operates and where it is headed. Cap now works almost exclusively on medical device issues at Olsson, Frank and Weeda (OFW Law in Washington, D.C. Date, Venue and Price: Location: Los Angeles, CA Date: August 21st & 22nd, 2014 Time: 9 AM to 6 PM Venue: DoubleTree by Hilton Hotel Los Angeles Downtown Address: 120 South Los Angeles Street, Los Angeles, California, 90012, USA Price: $1295.00 (Seminar for One Delegate) Discount: Register now and save $200. (Early Bird) Until July10, Early Bird Price: $1,295.00, From July 11 to August 19, Regular Price: $1,495.00 Want to register by Wire Transfer? Please call any of our representatives on 1800 447 9407 to help you completed the transfer. Contact Information: John Robinson Toll free: 1800 447 9407 Fax: 302 288 6884 Email: support@globalcompliancepanel.com Website: https://www.globalcompliancepanel.com Live Chat - Online Help Desk: http://www.globalcompliancepanel.com/chat/client.php GlobalCompliancePanel NetZealous LLC 161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA For More Info on This Seminar Kindly Go through the Below Link: http://bit.ly/FDAsBorderPatrolService To Download Seminar Boucher: http://bit.ly/FDAImportProcess GlobalCompliancePanel Seminar Gallery: http://bit.ly/1mCjvMb