2-day In-person Seminar
Tougher Import Rules for FDA Imports in 2018
Time: 9:00 AM to 6:00 PM
Venue: Courtyard Seattle Sea-Tac Area
**Please note the registration will be closed 2 days (48 Hours) prior to the date of the seminar.
Why you should 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. CBP is implemented a new "Automated Commercial Environment" computer program that changes import logistics and information reporting for FDA regulated products. Your shipment may be stopped before it is even loaded at the foreign port.
When products are refused, you have different options. Some options may cost more than others. For example, your product can be seized and 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.
Learn how to deal with common problems, such as returns for repair, importing QC samples, and investigational products
On a positive note, the FDA is implementing the Voluntary Qualification Importer Program under the FDA Food Safety and Modernization Act. One other perk is that FDA offers export certificates, for a modest fee, which may give you a competitive advantage in foreign markets. In some cases, a FDA export certificate is required by foreign governments. Finally, the new EU Medical Device Regulation will change how FDA manages foreign inspections and in your favor.
Who Will Benefit:
- Domestic importers
- Foreign exporter
- Initial importers
- International trade executives
- Venture Capitalists
- Marine insurance underwriters
- Import Brokers
- Regulatory affairs managers
- Import / Export consultants
- In-house counsel
- Contract specialists
- Logistics managers
- Third party establishment inspection entities
- Sales managers
- Investors
Day 1 Schedule
Lecture 1:
FDA Legal Authority Customs and Border Control (CBP) Import Process FDA Import Process Registration and documentation
Lecture 2:
FDA Import Process (continued)
- Import Brokers
- Prior Notice Information
- CBP and FDA computer programs
- Import Codes
- Bonds and Bonded Warehouses
- FDA "Notice of Action"
Lecture 3:
Import Delays Import Alerts Detention Refusals
Day 2 Schedule
Lecture 1:
Foreign Inspections FDA 483 - Inspectional Observations
Lecture 2:
FDA Warning Letters and Automatic detention
Lecture 3:
Import Hypothetical FDA Import for Export Program FDA Export Program Export Hypothetical
Lecture 4:
FDA Export Program Special Import Issues
- Trade Shows
- Personal Use
- Compassionate Use
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Group participations
Get fabulous discounts by participating in groups of two or more.| No | Attendees | Discount |
|---|---|---|
| 1 | 2 Attendees | 10% off |
| 2 | 3 to 6 Attendees | 20% off |
| 3 | 7 to 10 Attendees | 25% off |
| 4 | 10+ Attendees | 30% off |
To avail the above group discounts, all the participants should register by making a single payment
Call our representative TODAY on 1800 447 9407 to have your seats confirmed!
Casper Uldriks
ex-FDA Expert and former Associate Center Director of CDRHCasper (Cap) Uldriks owns Encore Insight LLC, which provides consulting services on FDA Law. He 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 Center Director for the Center 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, straightforward and of practical value. He understands how FDA thinks, operates and where it is headed.